<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX4440026" alias="SC_EXP_30328_3#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552364H, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GGTTTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552364H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440030" alias="SC_EXP_30328_3#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552368L, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GTAATCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552368L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440031" alias="SC_EXP_30328_3#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552369M, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TCCGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552369M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440032" alias="SC_EXP_30328_3#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552370F, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence AGTTCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552370F</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440033" alias="SC_EXP_30328_3#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552371G, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CAGCATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552371G</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440034" alias="SC_EXP_30328_3#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552372H, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CCACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552372H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440035" alias="SC_EXP_30328_3#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552373I, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence AACTGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552373I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440036" alias="SC_EXP_30328_3#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552374J, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TTGGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552374J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440037" alias="SC_EXP_30328_3#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552375K, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GGTAACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552375K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440038" alias="SC_EXP_30328_3#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552376L, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CACTCGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552376L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440039" alias="SC_EXP_30328_3#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552377M, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GCTGAATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552377M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440040" alias="SC_EXP_30328_3#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552378N, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TGAAGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552378N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440041" alias="SC_EXP_30328_3#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552379O, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence ATGCTCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552379O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440042" alias="SC_EXP_30328_3#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552380H, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TGGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552380H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440043" alias="SC_EXP_30328_3#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440043</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552381I, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GAAAGGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552381I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440044" alias="SC_EXP_30328_3#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552382J, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence ACTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552382J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440045" alias="SC_EXP_30328_3#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552383K, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CTCCTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552383K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440046" alias="SC_EXP_30328_3#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552384L, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GTTGCAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552384L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440047" alias="SC_EXP_30328_3#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552385M, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TGGAATTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552385M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440048" alias="SC_EXP_30328_3#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552386N, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CAATGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552386N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440049" alias="SC_EXP_30328_3#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552387O, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence ACCCTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552387O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440050" alias="SC_EXP_30328_3#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552388P, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence ATGAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552388P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440051" alias="SC_EXP_30328_3#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552389Q, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GATCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552389Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440052" alias="SC_EXP_30328_3#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552390J, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CCAGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552390J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440053" alias="SC_EXP_30328_3#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552391K, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552391K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440054" alias="SC_EXP_30328_3#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552392L, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GGCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552392L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440055" alias="SC_EXP_30328_3#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552393M, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence ACTTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552393M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440056" alias="SC_EXP_30328_3#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552394N, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CAAATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552394N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440057" alias="SC_EXP_30328_3#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552395O, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TTGCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552395O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440058" alias="SC_EXP_30328_3#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552396P, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence GTAATTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552396P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440059" alias="SC_EXP_30328_3#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552397Q, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence AGTCGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552397Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440060" alias="SC_EXP_30328_3#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552398R, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CACGAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552398R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440061" alias="SC_EXP_30328_3#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552399S, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TCGTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552399S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440062" alias="SC_EXP_30328_4#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552364H, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GGTTTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552364H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440063" alias="SC_EXP_30328_4#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552365I, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CTAAACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552365I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440064" alias="SC_EXP_30328_4#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552366J, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TCGGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552366J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440065" alias="SC_EXP_30328_4#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552367K, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence AACCGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552367K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440066" alias="SC_EXP_30328_4#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552368L, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GTAATCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552368L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440067" alias="SC_EXP_30328_4#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552369M, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TCCGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552369M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440068" alias="SC_EXP_30328_4#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552370F, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence AGTTCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552370F</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440069" alias="SC_EXP_30328_4#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552371G, constructed from sample accession ERS3535304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CAGCATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552371G</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440070" alias="SC_EXP_30328_4#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552372H, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CCACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552372H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440071" alias="SC_EXP_30328_4#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552373I, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence AACTGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552373I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440072" alias="SC_EXP_30328_4#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552374J, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TTGGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552374J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440073" alias="SC_EXP_30328_4#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552375K, constructed from sample accession ERS3535305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GGTAACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552375K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440074" alias="SC_EXP_30328_4#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552376L, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CACTCGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552376L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440075" alias="SC_EXP_30328_4#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552377M, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GCTGAATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552377M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440076" alias="SC_EXP_30328_4#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552378N, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TGAAGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552378N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440077" alias="SC_EXP_30328_4#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552379O, constructed from sample accession ERS3535306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence ATGCTCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552379O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440078" alias="SC_EXP_30328_4#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552380H, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TGGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552380H</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440079" alias="SC_EXP_30328_4#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552381I, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GAAAGGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552381I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440080" alias="SC_EXP_30328_4#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552382J, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence ACTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552382J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440081" alias="SC_EXP_30328_4#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552383K, constructed from sample accession ERS3535307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CTCCTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552383K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440082" alias="SC_EXP_30328_4#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552384L, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GTTGCAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552384L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440083" alias="SC_EXP_30328_4#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552385M, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TGGAATTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552385M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440084" alias="SC_EXP_30328_4#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552386N, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CAATGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552386N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440085" alias="SC_EXP_30328_4#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552387O, constructed from sample accession ERS3535308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence ACCCTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552387O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440086" alias="SC_EXP_30328_4#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552388P, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence ATGAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552388P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440087" alias="SC_EXP_30328_4#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552389Q, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GATCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552389Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440088" alias="SC_EXP_30328_4#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552390J, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CCAGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552390J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440089" alias="SC_EXP_30328_4#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552391K, constructed from sample accession ERS3535309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552391K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440090" alias="SC_EXP_30328_4#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552392L, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GGCGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552392L</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440091" alias="SC_EXP_30328_4#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552393M, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence ACTTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552393M</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440092" alias="SC_EXP_30328_4#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552394N, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CAAATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552394N</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440093" alias="SC_EXP_30328_4#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552395O, constructed from sample accession ERS3535310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TTGCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552395O</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440094" alias="SC_EXP_30328_4#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552396P, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence GTAATTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552396P</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440095" alias="SC_EXP_30328_4#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552397Q, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence AGTCGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552397Q</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440096" alias="SC_EXP_30328_4#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552398R, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence CACGAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552398R</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440097" alias="SC_EXP_30328_4#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_4#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_4#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552399S, constructed from sample accession ERS3535311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_4).  This submission includes reads tagged with the sequence TCGTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552399S</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440098" alias="SC_EXP_30501_1#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A1, constructed from sample accession ERS3459897 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459897">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440099" alias="SC_EXP_30501_1#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B1, constructed from sample accession ERS3459898 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCGTTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459898">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440100" alias="SC_EXP_30501_1#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C1, constructed from sample accession ERS3459899 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTAACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459899">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440101" alias="SC_EXP_30501_1#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D1, constructed from sample accession ERS3459900 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCGACTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459900">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440102" alias="SC_EXP_30501_1#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E1, constructed from sample accession ERS3459901 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATTTATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459901">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440103" alias="SC_EXP_30501_1#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F1, constructed from sample accession ERS3459902 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTAAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440104" alias="SC_EXP_30501_1#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G1, constructed from sample accession ERS3459903 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTAGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459903">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440105" alias="SC_EXP_30501_1#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H1, constructed from sample accession ERS3459904 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459904">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440106" alias="SC_EXP_30501_1#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I1, constructed from sample accession ERS3459905 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTGATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440107" alias="SC_EXP_30501_1#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J1, constructed from sample accession ERS3459906 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCTCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459906">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459906</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440108" alias="SC_EXP_30501_1#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K1, constructed from sample accession ERS3459907 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TATTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459907">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459907</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440109" alias="SC_EXP_30501_1#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L1, constructed from sample accession ERS3459908 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCTCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440110" alias="SC_EXP_30501_1#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M1, constructed from sample accession ERS3459909 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTACGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459909">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459909</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440111" alias="SC_EXP_30501_1#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N1, constructed from sample accession ERS3459910 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCGGGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459910">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440112" alias="SC_EXP_30501_1#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O1, constructed from sample accession ERS3459911 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440113" alias="SC_EXP_30501_1#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P1, constructed from sample accession ERS3459912 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459912">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440114" alias="SC_EXP_30501_1#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A2, constructed from sample accession ERS3459913 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459913">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440115" alias="SC_EXP_30501_1#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B2, constructed from sample accession ERS3459914 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440116" alias="SC_EXP_30501_1#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C2, constructed from sample accession ERS3459915 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GATACTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459915">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440117" alias="SC_EXP_30501_1#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D2, constructed from sample accession ERS3459916 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459916">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440118" alias="SC_EXP_30501_1#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E2, constructed from sample accession ERS3459917 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCAAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440119" alias="SC_EXP_30501_1#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F2, constructed from sample accession ERS3459918 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTCGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459918">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440120" alias="SC_EXP_30501_1#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G2, constructed from sample accession ERS3459919 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCGGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459919">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440121" alias="SC_EXP_30501_1#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H2, constructed from sample accession ERS3459920 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTCATATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459920">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440122" alias="SC_EXP_30501_1#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I2, constructed from sample accession ERS3459921 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCTTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459921">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459921</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440123" alias="SC_EXP_30501_1#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J2, constructed from sample accession ERS3459922 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459922">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440124" alias="SC_EXP_30501_1#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K2, constructed from sample accession ERS3459923 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCACTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459923">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459923</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440125" alias="SC_EXP_30501_1#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L2, constructed from sample accession ERS3459924 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCGATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459924">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459924</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440126" alias="SC_EXP_30501_1#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M2, constructed from sample accession ERS3459925 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440127" alias="SC_EXP_30501_1#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N2, constructed from sample accession ERS3459926 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459926">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459926</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440128" alias="SC_EXP_30501_1#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O2, constructed from sample accession ERS3459927 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459927">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459927</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440129" alias="SC_EXP_30501_1#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P2, constructed from sample accession ERS3459928 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440130" alias="SC_EXP_30501_1#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A3, constructed from sample accession ERS3459929 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TATATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459929">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440131" alias="SC_EXP_30501_1#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B3, constructed from sample accession ERS3459930 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459930">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459930</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440132" alias="SC_EXP_30501_1#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C3, constructed from sample accession ERS3459931 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTATCCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440133" alias="SC_EXP_30501_1#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D3, constructed from sample accession ERS3459932 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCCACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459932">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459932</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440134" alias="SC_EXP_30501_1#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E3, constructed from sample accession ERS3459933 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTACCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459933">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440135" alias="SC_EXP_30501_1#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F3, constructed from sample accession ERS3459934 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCCTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440136" alias="SC_EXP_30501_1#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G3, constructed from sample accession ERS3459935 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAGAGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459935">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440137" alias="SC_EXP_30501_1#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H3, constructed from sample accession ERS3459936 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTCGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459936">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459936</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440138" alias="SC_EXP_30501_1#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I3, constructed from sample accession ERS3459937 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459937">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440139" alias="SC_EXP_30501_1#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J3, constructed from sample accession ERS3459938 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGACGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440140" alias="SC_EXP_30501_1#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K3, constructed from sample accession ERS3459939 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTCCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459939">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440141" alias="SC_EXP_30501_1#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L3, constructed from sample accession ERS3459940 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGTGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440142" alias="SC_EXP_30501_1#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M3, constructed from sample accession ERS3459941 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TAGGCGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440143" alias="SC_EXP_30501_1#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N3, constructed from sample accession ERS3459942 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTCAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440144" alias="SC_EXP_30501_1#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O3, constructed from sample accession ERS3459943 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GACTTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440145" alias="SC_EXP_30501_1#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P3, constructed from sample accession ERS3459944 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACTCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440146" alias="SC_EXP_30501_1#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A4, constructed from sample accession ERS3459945 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGCTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440147" alias="SC_EXP_30501_1#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B4, constructed from sample accession ERS3459946 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GACTATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440148" alias="SC_EXP_30501_1#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C4, constructed from sample accession ERS3459947 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGTGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440149" alias="SC_EXP_30501_1#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D4, constructed from sample accession ERS3459948 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440150" alias="SC_EXP_30501_1#53">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E4, constructed from sample accession ERS3459949 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACAAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440151" alias="SC_EXP_30501_1#54">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F4, constructed from sample accession ERS3459950 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440152" alias="SC_EXP_30501_1#55">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G4, constructed from sample accession ERS3459951 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTAACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440153" alias="SC_EXP_30501_1#56">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H4, constructed from sample accession ERS3459952 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCGGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440154" alias="SC_EXP_30501_1#57">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I4, constructed from sample accession ERS3459953 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGCGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440155" alias="SC_EXP_30501_1#58">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J4, constructed from sample accession ERS3459954 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCCTGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440156" alias="SC_EXP_30501_1#59">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K4, constructed from sample accession ERS3459955 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCACGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459955">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440157" alias="SC_EXP_30501_1#60">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L4, constructed from sample accession ERS3459956 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCTAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440158" alias="SC_EXP_30501_1#61">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M4, constructed from sample accession ERS3459957 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAACCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459957">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440159" alias="SC_EXP_30501_1#62">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N4, constructed from sample accession ERS3459958 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTCCAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440160" alias="SC_EXP_30501_1#63">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O4, constructed from sample accession ERS3459959 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATGGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459959">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440161" alias="SC_EXP_30501_1#64">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P4, constructed from sample accession ERS3459960 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GATTAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440162" alias="SC_EXP_30501_1#65">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A5, constructed from sample accession ERS3459961 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCATCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440163" alias="SC_EXP_30501_1#66">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B5, constructed from sample accession ERS3459962 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCATGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440164" alias="SC_EXP_30501_1#67">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C5, constructed from sample accession ERS3459963 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACTTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440165" alias="SC_EXP_30501_1#68">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D5, constructed from sample accession ERS3459964 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCTTGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440166" alias="SC_EXP_30501_1#69">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E5, constructed from sample accession ERS3459965 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTAAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440167" alias="SC_EXP_30501_1#70">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F5, constructed from sample accession ERS3459966 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440168" alias="SC_EXP_30501_1#71">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G5, constructed from sample accession ERS3459967 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440169" alias="SC_EXP_30501_1#72">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H5, constructed from sample accession ERS3459968 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTTCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440170" alias="SC_EXP_30501_1#73">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I5, constructed from sample accession ERS3459969 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTCCGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440171" alias="SC_EXP_30501_1#74">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J5, constructed from sample accession ERS3459970 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTATATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440172" alias="SC_EXP_30501_1#75">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K5, constructed from sample accession ERS3459971 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCGCTAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440173" alias="SC_EXP_30501_1#76">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L5, constructed from sample accession ERS3459972 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCTAAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459972">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440174" alias="SC_EXP_30501_1#77">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M5, constructed from sample accession ERS3459973 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCCACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459973">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440175" alias="SC_EXP_30501_1#78">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N5, constructed from sample accession ERS3459974 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCGCCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440176" alias="SC_EXP_30501_1#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O5, constructed from sample accession ERS3459975 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AACTTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440177" alias="SC_EXP_30501_1#80">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P5, constructed from sample accession ERS3459976 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTGGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459976">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440178" alias="SC_EXP_30501_1#81">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A6, constructed from sample accession ERS3459977 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGATTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440179" alias="SC_EXP_30501_1#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B6, constructed from sample accession ERS3459978 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACGCCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459978">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440180" alias="SC_EXP_30501_1#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C6, constructed from sample accession ERS3459979 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AACTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459979">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440181" alias="SC_EXP_30501_1#84">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D6, constructed from sample accession ERS3459980 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCCTATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440182" alias="SC_EXP_30501_1#85">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E6, constructed from sample accession ERS3459981 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AAACGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459981">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440183" alias="SC_EXP_30501_1#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F6, constructed from sample accession ERS3459982 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459982">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440184" alias="SC_EXP_30501_1#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G6, constructed from sample accession ERS3459983 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCTCGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440185" alias="SC_EXP_30501_1#88">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H6, constructed from sample accession ERS3459984 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TACGGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440186" alias="SC_EXP_30501_1#89">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I6, constructed from sample accession ERS3459985 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTCGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440187" alias="SC_EXP_30501_1#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J6, constructed from sample accession ERS3459986 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440188" alias="SC_EXP_30501_1#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K6, constructed from sample accession ERS3459987 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCACGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440189" alias="SC_EXP_30501_1#92">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L6, constructed from sample accession ERS3459988 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGGGTTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440190" alias="SC_EXP_30501_1#93">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M6, constructed from sample accession ERS3459989 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGGCTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440191" alias="SC_EXP_30501_1#94">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N6, constructed from sample accession ERS3459990 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGATCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459990">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440192" alias="SC_EXP_30501_1#95">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O6, constructed from sample accession ERS3459991 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCTGTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440193" alias="SC_EXP_30501_1#96">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P6, constructed from sample accession ERS3459992 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCGTACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459992">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459992</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440194" alias="SC_EXP_30501_1#97">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#97</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A7, constructed from sample accession ERS3459993 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTAACTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440195" alias="SC_EXP_30501_1#98">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B7, constructed from sample accession ERS3459994 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440196" alias="SC_EXP_30501_1#99">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C7, constructed from sample accession ERS3459995 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTGCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440197" alias="SC_EXP_30501_1#100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D7, constructed from sample accession ERS3459996 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCTGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440198" alias="SC_EXP_30501_1#101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#101</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E7, constructed from sample accession ERS3459997 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTAGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440199" alias="SC_EXP_30501_1#102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F7, constructed from sample accession ERS3459998 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACGTTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459998">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459998</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440200" alias="SC_EXP_30501_1#103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G7, constructed from sample accession ERS3459999 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTGGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3459999">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3459999</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440201" alias="SC_EXP_30501_1#104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H7, constructed from sample accession ERS3460000 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCTTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440202" alias="SC_EXP_30501_1#105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I7, constructed from sample accession ERS3460001 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ATATGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460001">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460001</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440203" alias="SC_EXP_30501_1#106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J7, constructed from sample accession ERS3460002 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGACGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460002">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460002</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440204" alias="SC_EXP_30501_1#107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K7, constructed from sample accession ERS3460003 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460003">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440205" alias="SC_EXP_30501_1#108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L7, constructed from sample accession ERS3460004 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460004">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460004</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440206" alias="SC_EXP_30501_1#109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M7, constructed from sample accession ERS3460005 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGCCTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460005">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440207" alias="SC_EXP_30501_1#110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N7, constructed from sample accession ERS3460006 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGCATCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440208" alias="SC_EXP_30501_1#111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O7, constructed from sample accession ERS3460007 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGATAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460007">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460007</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440209" alias="SC_EXP_30501_1#112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P7, constructed from sample accession ERS3460008 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440210" alias="SC_EXP_30501_1#113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#113</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A8, constructed from sample accession ERS3460009 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460009">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440211" alias="SC_EXP_30501_1#114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B8, constructed from sample accession ERS3460010 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCATCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440212" alias="SC_EXP_30501_1#115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C8, constructed from sample accession ERS3460011 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440213" alias="SC_EXP_30501_1#116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#116</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D8, constructed from sample accession ERS3460012 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCGGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460012">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440214" alias="SC_EXP_30501_1#117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#117</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E8, constructed from sample accession ERS3460013 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAGAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460013">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440215" alias="SC_EXP_30501_1#118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#118</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F8, constructed from sample accession ERS3460014 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGCAAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440216" alias="SC_EXP_30501_1#119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#119</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G8, constructed from sample accession ERS3460015 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAAACCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440217" alias="SC_EXP_30501_1#120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#120</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H8, constructed from sample accession ERS3460016 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440218" alias="SC_EXP_30501_1#121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#121</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I8, constructed from sample accession ERS3460017 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAGACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460017">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440219" alias="SC_EXP_30501_1#122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J8, constructed from sample accession ERS3460018 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440220" alias="SC_EXP_30501_1#123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K8, constructed from sample accession ERS3460019 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460019">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440221" alias="SC_EXP_30501_1#124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L8, constructed from sample accession ERS3460020 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCGGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460020">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460020</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655994</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440222" alias="SC_EXP_30501_1#125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#125</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M8, constructed from sample accession ERS3460021 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCCGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655995</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440223" alias="SC_EXP_30501_1#126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#126</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N8, constructed from sample accession ERS3460022 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460022">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440224" alias="SC_EXP_30501_1#127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O8, constructed from sample accession ERS3460023 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460023">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440225" alias="SC_EXP_30501_1#128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P8, constructed from sample accession ERS3460024 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTAGATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440226" alias="SC_EXP_30501_1#129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#129</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A9, constructed from sample accession ERS3460025 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTCGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460025">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5655999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440227" alias="SC_EXP_30501_1#130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#130</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B9, constructed from sample accession ERS3460026 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460026">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440228" alias="SC_EXP_30501_1#131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#131</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C9, constructed from sample accession ERS3460027 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440229" alias="SC_EXP_30501_1#132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D9, constructed from sample accession ERS3460028 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460028">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440230" alias="SC_EXP_30501_1#133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#133</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E9, constructed from sample accession ERS3460029 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCATGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440231" alias="SC_EXP_30501_1#134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#134</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F9, constructed from sample accession ERS3460030 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTAATCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440232" alias="SC_EXP_30501_1#135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#135</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G9, constructed from sample accession ERS3460031 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGTACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460031">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440233" alias="SC_EXP_30501_1#136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H9, constructed from sample accession ERS3460032 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTATGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440234" alias="SC_EXP_30501_1#137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#137</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I9, constructed from sample accession ERS3460033 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTAAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440235" alias="SC_EXP_30501_1#138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#138</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J9, constructed from sample accession ERS3460034 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTATGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460034">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440236" alias="SC_EXP_30501_1#139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K9, constructed from sample accession ERS3460035 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460035">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440237" alias="SC_EXP_30501_1#140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L9, constructed from sample accession ERS3460036 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGTTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440238" alias="SC_EXP_30501_1#141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#141</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M9, constructed from sample accession ERS3460037 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GACGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460037">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440239" alias="SC_EXP_30501_1#142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#142</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N9, constructed from sample accession ERS3460038 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TATATTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460038">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656012</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440240" alias="SC_EXP_30501_1#143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O9, constructed from sample accession ERS3460039 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGCTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440241" alias="SC_EXP_30501_1#144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P9, constructed from sample accession ERS3460040 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGACCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460040">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656014</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440242" alias="SC_EXP_30501_1#145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#145</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A10, constructed from sample accession ERS3460041 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTCTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460041">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656015</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440243" alias="SC_EXP_30501_1#146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#146</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B10, constructed from sample accession ERS3460042 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCGGGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440244" alias="SC_EXP_30501_1#147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C10, constructed from sample accession ERS3460043 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656017</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440245" alias="SC_EXP_30501_1#148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D10, constructed from sample accession ERS3460044 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACGTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460044">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440246" alias="SC_EXP_30501_1#149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#149</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E10, constructed from sample accession ERS3460048 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAAACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460048">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440247" alias="SC_EXP_30501_1#150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#150</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F10, constructed from sample accession ERS3460049 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGTATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440248" alias="SC_EXP_30501_1#151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#151</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G10, constructed from sample accession ERS3460050 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCCATTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460050">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440249" alias="SC_EXP_30501_1#152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H10, constructed from sample accession ERS3460051 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCGTTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460051">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440250" alias="SC_EXP_30501_1#153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#153</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I10, constructed from sample accession ERS3460052 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440251" alias="SC_EXP_30501_1#154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#154</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J10, constructed from sample accession ERS3460053 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGCTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440252" alias="SC_EXP_30501_1#155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K10, constructed from sample accession ERS3460054 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCCAAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460054">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440253" alias="SC_EXP_30501_1#156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L10, constructed from sample accession ERS3460055 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTCGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440254" alias="SC_EXP_30501_1#157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#157</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M10, constructed from sample accession ERS3460045 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACTGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460045">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440255" alias="SC_EXP_30501_1#158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#158</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N10, constructed from sample accession ERS3460046 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440256" alias="SC_EXP_30501_1#159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#159</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O10, constructed from sample accession ERS3460047 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAGGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656021</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440257" alias="SC_EXP_30501_1#160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P10, constructed from sample accession ERS3460056 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AACCAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440258" alias="SC_EXP_30501_1#161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#161</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A11, constructed from sample accession ERS3460057 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440259" alias="SC_EXP_30501_1#162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#162</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B11, constructed from sample accession ERS3460058 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460058">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440260" alias="SC_EXP_30501_1#163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C11, constructed from sample accession ERS3460059 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460059">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460059</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440261" alias="SC_EXP_30501_1#164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D11, constructed from sample accession ERS3460060 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTGGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460060">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460060</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440262" alias="SC_EXP_30501_1#165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#165</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E11, constructed from sample accession ERS3460061 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GATATGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460061">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460061</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440263" alias="SC_EXP_30501_1#166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#166</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F11, constructed from sample accession ERS3460062 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCGAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460062">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460062</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440264" alias="SC_EXP_30501_1#167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#167</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G11, constructed from sample accession ERS3460063 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460063">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460063</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440265" alias="SC_EXP_30501_1#168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H11, constructed from sample accession ERS3460064 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTCGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460064">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460064</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440266" alias="SC_EXP_30501_1#169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#169</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I11, constructed from sample accession ERS3460065 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460065">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460065</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440267" alias="SC_EXP_30501_1#170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#170</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J11, constructed from sample accession ERS3460066 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ATCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460066">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460066</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440268" alias="SC_EXP_30501_1#171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K11, constructed from sample accession ERS3460067 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460067">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460067</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440269" alias="SC_EXP_30501_1#172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#172</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L11, constructed from sample accession ERS3460068 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGGGCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460068">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460068</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440270" alias="SC_EXP_30501_1#173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#173</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M11, constructed from sample accession ERS3460069 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCGGCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460069">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440271" alias="SC_EXP_30501_1#174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#174</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N11, constructed from sample accession ERS3460070 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGCACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460070">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460070</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440272" alias="SC_EXP_30501_1#175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O11, constructed from sample accession ERS3460071 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460071">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460071</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440273" alias="SC_EXP_30501_1#176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P11, constructed from sample accession ERS3460072 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAAATAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460072">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460072</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440274" alias="SC_EXP_30501_1#177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#177</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A12, constructed from sample accession ERS3460073 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460073">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460073</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440275" alias="SC_EXP_30501_1#178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#178</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B12, constructed from sample accession ERS3460074 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460074">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460074</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440276" alias="SC_EXP_30501_1#179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#179</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C12, constructed from sample accession ERS3460075 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAAAGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460075">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460075</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440277" alias="SC_EXP_30501_1#180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D12, constructed from sample accession ERS3460076 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCAAAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460076">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460076</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440278" alias="SC_EXP_30501_1#181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#181</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E12, constructed from sample accession ERS3460077 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGACGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460077">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460077</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440279" alias="SC_EXP_30501_1#182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#182</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F12, constructed from sample accession ERS3460078 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCTTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460078">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460078</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440280" alias="SC_EXP_30501_1#183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#183</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G12, constructed from sample accession ERS3460079 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGAAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460079">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460079</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440281" alias="SC_EXP_30501_1#184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#184</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H12, constructed from sample accession ERS3460080 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAGGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460080">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460080</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440282" alias="SC_EXP_30501_1#185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#185</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I12, constructed from sample accession ERS3460081 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460081">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460081</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440283" alias="SC_EXP_30501_1#186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#186</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J12, constructed from sample accession ERS3460082 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCGGGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460082">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440284" alias="SC_EXP_30501_1#187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#187</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K12, constructed from sample accession ERS3460083 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGTTGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460083">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440285" alias="SC_EXP_30501_1#188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#188</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L12, constructed from sample accession ERS3460084 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440286" alias="SC_EXP_30501_1#189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#189</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M12, constructed from sample accession ERS3460085 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCCTTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440287" alias="SC_EXP_30501_1#190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#190</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N12, constructed from sample accession ERS3460086 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCCGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440288" alias="SC_EXP_30501_1#191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#191</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O12, constructed from sample accession ERS3460087 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAGAAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440289" alias="SC_EXP_30501_1#192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#192</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P12, constructed from sample accession ERS3460088 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAAATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460088">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440290" alias="SC_EXP_30501_1#193">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#193</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#193</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A13, constructed from sample accession ERS3460089 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTACCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460089">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440291" alias="SC_EXP_30501_1#194">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#194</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B13, constructed from sample accession ERS3460090 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTTCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460090">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440292" alias="SC_EXP_30501_1#195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#195</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C13, constructed from sample accession ERS3460091 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TACGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460091">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440293" alias="SC_EXP_30501_1#196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#196</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D13, constructed from sample accession ERS3460092 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460092">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440294" alias="SC_EXP_30501_1#197">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#197</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E13, constructed from sample accession ERS3460093 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTCGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460093">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440295" alias="SC_EXP_30501_1#198">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#198</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F13, constructed from sample accession ERS3460094 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AATAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460094">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440296" alias="SC_EXP_30501_1#199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#199</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G13, constructed from sample accession ERS3460095 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCACTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460095">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440297" alias="SC_EXP_30501_1#200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#200</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H13, constructed from sample accession ERS3460096 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460096">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440298" alias="SC_EXP_30501_1#201">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#201</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I13, constructed from sample accession ERS3460097 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGATGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440299" alias="SC_EXP_30501_1#202">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#202</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#202</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J13, constructed from sample accession ERS3460098 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCGTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440300" alias="SC_EXP_30501_1#203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#203</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K13, constructed from sample accession ERS3460099 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460099">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656073</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440301" alias="SC_EXP_30501_1#204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#204</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L13, constructed from sample accession ERS3460100 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGACTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460100">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440302" alias="SC_EXP_30501_1#205">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#205</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#205</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M13, constructed from sample accession ERS3460101 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TAGTATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460101">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460101</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656075</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440303" alias="SC_EXP_30501_1#206">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#206</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N13, constructed from sample accession ERS3460102 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGGGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460102">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440304" alias="SC_EXP_30501_1#207">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#207</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O13, constructed from sample accession ERS3460103 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGACACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460103">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656077</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440305" alias="SC_EXP_30501_1#208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#208</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P13, constructed from sample accession ERS3460104 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GATATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460104">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460104</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656078</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440306" alias="SC_EXP_30501_1#209">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#209</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A14, constructed from sample accession ERS3460105 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656079</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440307" alias="SC_EXP_30501_1#210">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#210</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B14, constructed from sample accession ERS3460106 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440308" alias="SC_EXP_30501_1#211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#211</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C14, constructed from sample accession ERS3460107 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTTGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460107">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656081</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440309" alias="SC_EXP_30501_1#212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#212</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D14, constructed from sample accession ERS3460108 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440310" alias="SC_EXP_30501_1#213">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#213</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#213</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E14, constructed from sample accession ERS3460109 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGGGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656083</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440311" alias="SC_EXP_30501_1#214">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#214</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F14, constructed from sample accession ERS3460110 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCGGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440312" alias="SC_EXP_30501_1#215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#215</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G14, constructed from sample accession ERS3460111 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GACGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440313" alias="SC_EXP_30501_1#216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#216</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H14, constructed from sample accession ERS3460112 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCGGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440314" alias="SC_EXP_30501_1#217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#217</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I14, constructed from sample accession ERS3460113 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCTTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440315" alias="SC_EXP_30501_1#218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#218</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J14, constructed from sample accession ERS3460114 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440316" alias="SC_EXP_30501_1#219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#219</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K14, constructed from sample accession ERS3460115 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTTCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440317" alias="SC_EXP_30501_1#220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#220</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L14, constructed from sample accession ERS3460116 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AACGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656090</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440318" alias="SC_EXP_30501_1#221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#221</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M14, constructed from sample accession ERS3460117 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGCACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440319" alias="SC_EXP_30501_1#222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#222</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#222</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N14, constructed from sample accession ERS3460118 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440320" alias="SC_EXP_30501_1#223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#223</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O14, constructed from sample accession ERS3460119 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440321" alias="SC_EXP_30501_1#224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#224</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P14, constructed from sample accession ERS3460120 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440322" alias="SC_EXP_30501_1#225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#225</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A15, constructed from sample accession ERS3460121 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGTAGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440323" alias="SC_EXP_30501_1#226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#226</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#226</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B15, constructed from sample accession ERS3460122 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AATGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440324" alias="SC_EXP_30501_1#227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#227</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C15, constructed from sample accession ERS3460123 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440325" alias="SC_EXP_30501_1#228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#228</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D15, constructed from sample accession ERS3460124 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCAATAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440326" alias="SC_EXP_30501_1#229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#229</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E15, constructed from sample accession ERS3460125 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTGTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440327" alias="SC_EXP_30501_1#230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#230</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F15, constructed from sample accession ERS3460126 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440328" alias="SC_EXP_30501_1#231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#231</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#231</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G15, constructed from sample accession ERS3460127 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440329" alias="SC_EXP_30501_1#232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#232</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H15, constructed from sample accession ERS3460128 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440330" alias="SC_EXP_30501_1#233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#233</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I15, constructed from sample accession ERS3460129 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTGCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440331" alias="SC_EXP_30501_1#234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#234</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J15, constructed from sample accession ERS3460130 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCGCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440332" alias="SC_EXP_30501_1#235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#235</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K15, constructed from sample accession ERS3460131 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATATTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440333" alias="SC_EXP_30501_1#236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#236</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L15, constructed from sample accession ERS3460132 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCAAACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440334" alias="SC_EXP_30501_1#237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#237</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M15, constructed from sample accession ERS3460133 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCCTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460133">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440335" alias="SC_EXP_30501_1#238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#238</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N15, constructed from sample accession ERS3460134 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCGATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440336" alias="SC_EXP_30501_1#239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#239</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O15, constructed from sample accession ERS3460135 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GACTCCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440337" alias="SC_EXP_30501_1#240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#240</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P15, constructed from sample accession ERS3460136 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440338" alias="SC_EXP_30501_1#241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#241</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A16, constructed from sample accession ERS3460137 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440339" alias="SC_EXP_30501_1#242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#242</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#242</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B16, constructed from sample accession ERS3460138 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCTTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460138">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440340" alias="SC_EXP_30501_1#243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#243</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#243</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C16, constructed from sample accession ERS3460139 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTCACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460139">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440341" alias="SC_EXP_30501_1#244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#244</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#244</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D16, constructed from sample accession ERS3460140 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGGCCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460140">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440342" alias="SC_EXP_30501_1#245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#245</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E16, constructed from sample accession ERS3460141 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGGCTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460141">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440343" alias="SC_EXP_30501_1#246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#246</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F16, constructed from sample accession ERS3460142 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCTGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460142">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440344" alias="SC_EXP_30501_1#247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#247</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G16, constructed from sample accession ERS3460143 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCTCTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460143">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440345" alias="SC_EXP_30501_1#248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#248</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H16, constructed from sample accession ERS3460144 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCGGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460144">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440346" alias="SC_EXP_30501_1#249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#249</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I16, constructed from sample accession ERS3460145 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460145">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440347" alias="SC_EXP_30501_1#250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#250</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J16, constructed from sample accession ERS3460146 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460146">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440348" alias="SC_EXP_30501_1#251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#251</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K16, constructed from sample accession ERS3460147 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCGCATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440349" alias="SC_EXP_30501_1#252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#252</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L16, constructed from sample accession ERS3460148 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGACGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460148">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440350" alias="SC_EXP_30501_1#253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#253</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M16, constructed from sample accession ERS3460149 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460149">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440351" alias="SC_EXP_30501_1#254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#254</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N16, constructed from sample accession ERS3460150 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTAAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440352" alias="SC_EXP_30501_1#255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#255</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O16, constructed from sample accession ERS3460151 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTCTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460151">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440353" alias="SC_EXP_30501_1#256">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#256</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#256</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P16, constructed from sample accession ERS3460152 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTTCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460152">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440354" alias="SC_EXP_30501_1#257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#257</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A17, constructed from sample accession ERS3460153 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCACGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460153">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440355" alias="SC_EXP_30501_1#258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#258</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B17, constructed from sample accession ERS3460154 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460154">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440356" alias="SC_EXP_30501_1#259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#259</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C17, constructed from sample accession ERS3460155 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCTGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460155">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440357" alias="SC_EXP_30501_1#260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#260</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D17, constructed from sample accession ERS3460156 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCTGAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460156">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440358" alias="SC_EXP_30501_1#261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#261</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E17, constructed from sample accession ERS3460157 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCAGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460157">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440359" alias="SC_EXP_30501_1#262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#262</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#262</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F17, constructed from sample accession ERS3460158 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGAAAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460158">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440360" alias="SC_EXP_30501_1#263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#263</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#263</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G17, constructed from sample accession ERS3460159 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460159">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440361" alias="SC_EXP_30501_1#264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#264</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#264</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H17, constructed from sample accession ERS3460160 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGGTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460160">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460160</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440362" alias="SC_EXP_30501_1#265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#265</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#265</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I17, constructed from sample accession ERS3460161 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460161">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440363" alias="SC_EXP_30501_1#266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#266</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#266</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J17, constructed from sample accession ERS3460162 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460162">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460162</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440364" alias="SC_EXP_30501_1#267">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#267</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#267</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K17, constructed from sample accession ERS3460163 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TATCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460163">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440365" alias="SC_EXP_30501_1#268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#268</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#268</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L17, constructed from sample accession ERS3460164 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCAGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440366" alias="SC_EXP_30501_1#269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#269</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M17, constructed from sample accession ERS3460165 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACTGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460165">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460165</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440367" alias="SC_EXP_30501_1#270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#270</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#270</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N17, constructed from sample accession ERS3460166 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGGGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460166">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460166</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440368" alias="SC_EXP_30501_1#271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#271</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#271</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O17, constructed from sample accession ERS3460167 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGAGTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460167">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440369" alias="SC_EXP_30501_1#272">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#272</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#272</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P17, constructed from sample accession ERS3460168 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460168">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440370" alias="SC_EXP_30501_1#273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#273</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A18, constructed from sample accession ERS3460169 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGGCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460169">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460169</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440371" alias="SC_EXP_30501_1#274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#274</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#274</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B18, constructed from sample accession ERS3460170 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTGAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460170">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440372" alias="SC_EXP_30501_1#275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#275</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#275</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C18, constructed from sample accession ERS3460171 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCGCTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460171">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460171</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440373" alias="SC_EXP_30501_1#276">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#276</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#276</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D18, constructed from sample accession ERS3460172 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCCTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460172">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440374" alias="SC_EXP_30501_1#277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#277</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#277</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E18, constructed from sample accession ERS3460173 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTGCGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460173">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440375" alias="SC_EXP_30501_1#278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#278</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#278</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F18, constructed from sample accession ERS3460174 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AAAGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460174">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440376" alias="SC_EXP_30501_1#279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#279</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#279</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G18, constructed from sample accession ERS3460175 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCCGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460175">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440377" alias="SC_EXP_30501_1#280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#280</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#280</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H18, constructed from sample accession ERS3460176 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACTCGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460176">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440378" alias="SC_EXP_30501_1#281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#281</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I18, constructed from sample accession ERS3460177 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AACCGGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460177">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440379" alias="SC_EXP_30501_1#282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#282</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#282</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J18, constructed from sample accession ERS3460178 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGATTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460178">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440380" alias="SC_EXP_30501_1#283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#283</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#283</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K18, constructed from sample accession ERS3460179 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460179">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440381" alias="SC_EXP_30501_1#284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#284</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#284</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L18, constructed from sample accession ERS3460180 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTAAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460180">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460180</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440382" alias="SC_EXP_30501_1#285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#285</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M18, constructed from sample accession ERS3460181 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCTAGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460181">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460181</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440383" alias="SC_EXP_30501_1#286">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#286</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#286</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N18, constructed from sample accession ERS3460182 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCTTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460182">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460182</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440384" alias="SC_EXP_30501_1#287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#287</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#287</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O18, constructed from sample accession ERS3460183 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTATTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460183">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460183</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440385" alias="SC_EXP_30501_1#288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#288</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#288</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P18, constructed from sample accession ERS3460184 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460184">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440386" alias="SC_EXP_30501_1#289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#289</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#289</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A19, constructed from sample accession ERS3460185 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCGGAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460185">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440387" alias="SC_EXP_30501_1#290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#290</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#290</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B19, constructed from sample accession ERS3460186 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTGACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460186">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440388" alias="SC_EXP_30501_1#291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#291</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#291</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C19, constructed from sample accession ERS3460187 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTGGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460187">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440389" alias="SC_EXP_30501_1#292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#292</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#292</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D19, constructed from sample accession ERS3460188 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460188">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440390" alias="SC_EXP_30501_1#293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#293</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E19, constructed from sample accession ERS3460189 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTCAAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460189">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460189</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440391" alias="SC_EXP_30501_1#294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#294</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F19, constructed from sample accession ERS3460190 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460190">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460190</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440392" alias="SC_EXP_30501_1#295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#295</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G19, constructed from sample accession ERS3460191 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460191">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440393" alias="SC_EXP_30501_1#296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#296</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H19, constructed from sample accession ERS3460192 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460192">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460192</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440394" alias="SC_EXP_30501_1#297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#297</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I19, constructed from sample accession ERS3460193 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCTAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460193">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460193</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440395" alias="SC_EXP_30501_1#298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J19, constructed from sample accession ERS3460194 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCGTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460194">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460194</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440396" alias="SC_EXP_30501_1#299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K19, constructed from sample accession ERS3460195 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGAGGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460195">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440397" alias="SC_EXP_30501_1#300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L19, constructed from sample accession ERS3460196 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTAGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460196">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460196</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440398" alias="SC_EXP_30501_1#301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M19, constructed from sample accession ERS3460197 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGCGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460197">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460197</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440399" alias="SC_EXP_30501_1#302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N19, constructed from sample accession ERS3460198 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACGCGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460198">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460198</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440400" alias="SC_EXP_30501_1#303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#303</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O19, constructed from sample accession ERS3460199 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCGCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460199">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460199</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440401" alias="SC_EXP_30501_1#304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#304</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P19, constructed from sample accession ERS3460200 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460200">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460200</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440402" alias="SC_EXP_30501_1#305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#305</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A20, constructed from sample accession ERS3460201 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGTGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460201">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460201</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440403" alias="SC_EXP_30501_1#306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#306</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B20, constructed from sample accession ERS3460202 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460202">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460202</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440404" alias="SC_EXP_30501_1#307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#307</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C20, constructed from sample accession ERS3460203 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460203">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460203</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440405" alias="SC_EXP_30501_1#308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D20, constructed from sample accession ERS3460204 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460204">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460204</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440406" alias="SC_EXP_30501_1#309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E20, constructed from sample accession ERS3460205 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCAAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460205">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460205</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440407" alias="SC_EXP_30501_1#310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F20, constructed from sample accession ERS3460206 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence ACGTAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460206">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460206</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440408" alias="SC_EXP_30501_1#311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G20, constructed from sample accession ERS3460207 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCTATATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460207">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460207</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440409" alias="SC_EXP_30501_1#312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H20, constructed from sample accession ERS3460208 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTTCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460208">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460208</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440410" alias="SC_EXP_30501_1#313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I20, constructed from sample accession ERS3460209 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCTGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460209">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460209</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440411" alias="SC_EXP_30501_1#314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J20, constructed from sample accession ERS3460210 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGACCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460210">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460210</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440412" alias="SC_EXP_30501_1#315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#315</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K20, constructed from sample accession ERS3460211 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGTATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440413" alias="SC_EXP_30501_1#316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#316</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L20, constructed from sample accession ERS3460212 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440414" alias="SC_EXP_30501_1#317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#317</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M20, constructed from sample accession ERS3460213 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460213">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460213</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440415" alias="SC_EXP_30501_1#318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#318</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#318</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N20, constructed from sample accession ERS3460214 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGCAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460214">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460214</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440416" alias="SC_EXP_30501_1#319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O20, constructed from sample accession ERS3460215 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGGATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460215">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460215</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440417" alias="SC_EXP_30501_1#320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P20, constructed from sample accession ERS3460216 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGCGGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460216">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460216</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440418" alias="SC_EXP_30501_1#321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A21, constructed from sample accession ERS3460217 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460217">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460217</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440419" alias="SC_EXP_30501_1#322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B21, constructed from sample accession ERS3460218 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTTGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656193</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440420" alias="SC_EXP_30501_1#323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C21, constructed from sample accession ERS3460219 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCAGGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440421" alias="SC_EXP_30501_1#324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#324</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D21, constructed from sample accession ERS3460220 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440422" alias="SC_EXP_30501_1#325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#325</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E21, constructed from sample accession ERS3460221 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTGTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656196</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440423" alias="SC_EXP_30501_1#326">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#326</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#326</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F21, constructed from sample accession ERS3460222 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTTAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460222">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460222</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440424" alias="SC_EXP_30501_1#327">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#327</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#327</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G21, constructed from sample accession ERS3460223 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AAGGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460223">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440425" alias="SC_EXP_30501_1#328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#328</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#328</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H21, constructed from sample accession ERS3460224 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460224">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460224</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656199</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440426" alias="SC_EXP_30501_1#329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#329</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#329</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I21, constructed from sample accession ERS3460225 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTACTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440427" alias="SC_EXP_30501_1#330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#330</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#330</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J21, constructed from sample accession ERS3460226 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCACGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440428" alias="SC_EXP_30501_1#331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#331</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#331</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K21, constructed from sample accession ERS3460227 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCGAATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460227">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460227</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440429" alias="SC_EXP_30501_1#332">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#332</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#332</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L21, constructed from sample accession ERS3460228 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GATGAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440430" alias="SC_EXP_30501_1#333">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#333</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#333</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M21, constructed from sample accession ERS3460229 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTTTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440431" alias="SC_EXP_30501_1#334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#334</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#334</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N21, constructed from sample accession ERS3460230 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460230">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460230</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440432" alias="SC_EXP_30501_1#335">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#335</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#335</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O21, constructed from sample accession ERS3460231 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440433" alias="SC_EXP_30501_1#336">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#336</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#336</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P21, constructed from sample accession ERS3460232 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AACCTGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440434" alias="SC_EXP_30501_1#337">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#337</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#337</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A22, constructed from sample accession ERS3460233 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTTTCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440435" alias="SC_EXP_30501_1#338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#338</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#338</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B22, constructed from sample accession ERS3460234 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AAATGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460234">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440436" alias="SC_EXP_30501_1#339">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#339</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#339</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C22, constructed from sample accession ERS3460235 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CATCGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440437" alias="SC_EXP_30501_1#340">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#340</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#340</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D22, constructed from sample accession ERS3460236 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCACAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440438" alias="SC_EXP_30501_1#341">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#341</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#341</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E22, constructed from sample accession ERS3460237 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AGACTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460237">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656212</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440439" alias="SC_EXP_30501_1#342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#342</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#342</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F22, constructed from sample accession ERS3460238 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AATGCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460238">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440440" alias="SC_EXP_30501_1#343">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#343</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#343</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G22, constructed from sample accession ERS3460239 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GACGGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460239">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656214</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440441" alias="SC_EXP_30501_1#344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#344</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#344</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H22, constructed from sample accession ERS3460240 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGATAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440442" alias="SC_EXP_30501_1#345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#345</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#345</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I22, constructed from sample accession ERS3460241 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TAGGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440443" alias="SC_EXP_30501_1#346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#346</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#346</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J22, constructed from sample accession ERS3460242 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GAGCATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460242">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440444" alias="SC_EXP_30501_1#347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#347</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#347</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K22, constructed from sample accession ERS3460243 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440445" alias="SC_EXP_30501_1#348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#348</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#348</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L22, constructed from sample accession ERS3460244 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTCTTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440446" alias="SC_EXP_30501_1#349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#349</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#349</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M22, constructed from sample accession ERS3460245 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTAGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656220</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440447" alias="SC_EXP_30501_1#350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#350</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#350</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N22, constructed from sample accession ERS3460246 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGCCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460246">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460246</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656221</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440448" alias="SC_EXP_30501_1#351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#351</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#351</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O22, constructed from sample accession ERS3460247 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGGAGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656222</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440449" alias="SC_EXP_30501_1#352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#352</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#352</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P22, constructed from sample accession ERS3460248 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460248">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440450" alias="SC_EXP_30501_1#353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#353</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#353</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A23, constructed from sample accession ERS3460249 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTGAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460249">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440451" alias="SC_EXP_30501_1#354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#354</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#354</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B23, constructed from sample accession ERS3460250 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTTAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460250">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440452" alias="SC_EXP_30501_1#355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#355</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#355</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C23, constructed from sample accession ERS3460251 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTTGGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656226</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440453" alias="SC_EXP_30501_1#356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#356</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#356</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D23, constructed from sample accession ERS3460252 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440454" alias="SC_EXP_30501_1#357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#357</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#357</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E23, constructed from sample accession ERS3460253 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AACAGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460253">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440455" alias="SC_EXP_30501_1#358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#358</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#358</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F23, constructed from sample accession ERS3460254 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTTGTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656229</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440456" alias="SC_EXP_30501_1#359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#359</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#359</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G23, constructed from sample accession ERS3460255 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AATTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440457" alias="SC_EXP_30501_1#360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#360</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#360</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H23, constructed from sample accession ERS3460256 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence AAAGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460256">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460256</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440458" alias="SC_EXP_30501_1#361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#361</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#361</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I23, constructed from sample accession ERS3460257 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGCATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440459" alias="SC_EXP_30501_1#362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#362</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#362</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J23, constructed from sample accession ERS3460258 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TCAGTTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440460" alias="SC_EXP_30501_1#363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#363</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#363</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K23, constructed from sample accession ERS3460259 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGTTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460259">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440461" alias="SC_EXP_30501_1#364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#364</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#364</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L23, constructed from sample accession ERS3460260 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460260">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460260</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440462" alias="SC_EXP_30501_1#365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440462</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#365</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#365</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M23, constructed from sample accession ERS3460261 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGGGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656236</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440463" alias="SC_EXP_30501_1#366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#366</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#366</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N23, constructed from sample accession ERS3460262 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCAGCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460262">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460262</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656237</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440464" alias="SC_EXP_30501_1#367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440464</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#367</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#367</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O23, constructed from sample accession ERS3460263 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGTGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440465" alias="SC_EXP_30501_1#368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440465</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#368</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#368</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P23, constructed from sample accession ERS3460264 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGCCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440466" alias="SC_EXP_30501_1#369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#369</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#369</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:A24, constructed from sample accession ERS3460265 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGCACCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460265">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460265</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656240</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440467" alias="SC_EXP_30501_1#370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#370</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#370</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:B24, constructed from sample accession ERS3460266 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CCGATCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:B24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440468" alias="SC_EXP_30501_1#371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#371</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#371</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:C24, constructed from sample accession ERS3460267 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CAAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460267">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460267</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656242</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440469" alias="SC_EXP_30501_1#372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#372</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#372</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:D24, constructed from sample accession ERS3460268 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GGCGTCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460268">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460268</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656243</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:D24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440470" alias="SC_EXP_30501_1#373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#373</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#373</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:E24, constructed from sample accession ERS3460269 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTAGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656244</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440471" alias="SC_EXP_30501_1#374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#374</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#374</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:F24, constructed from sample accession ERS3460270 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GTCGGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:F24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440472" alias="SC_EXP_30501_1#375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#375</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#375</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:G24, constructed from sample accession ERS3460271 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCCTCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460271">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656246</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440474" alias="SC_EXP_30501_1#377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#377</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#377</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:I24, constructed from sample accession ERS3460273 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TGGTCGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440475" alias="SC_EXP_30501_1#378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#378</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#378</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:J24, constructed from sample accession ERS3460274 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTAAACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656249</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:J24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440476" alias="SC_EXP_30501_1#379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#379</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#379</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:K24, constructed from sample accession ERS3460275 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CGTTGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656250</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440477" alias="SC_EXP_30501_1#380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#380</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#380</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:L24, constructed from sample accession ERS3460276 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CACTCTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:L24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440478" alias="SC_EXP_30501_1#381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#381</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#381</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:M24, constructed from sample accession ERS3460277 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TTGTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656252</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440479" alias="SC_EXP_30501_1#382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#382</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#382</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:N24, constructed from sample accession ERS3460278 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence GCAGCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656253</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:N24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440480" alias="SC_EXP_30501_1#383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#383</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#383</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:O24, constructed from sample accession ERS3460279 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTGCCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440481" alias="SC_EXP_30501_1#384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#384</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#384</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:P24, constructed from sample accession ERS3460280 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence TACCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656255</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:P24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440482" alias="SC_EXP_30598_1#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A1, constructed from sample accession ERS3460281 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656256</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440483" alias="SC_EXP_30598_1#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B1, constructed from sample accession ERS3460282 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCGTTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440484" alias="SC_EXP_30598_1#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C1, constructed from sample accession ERS3460283 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTAACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460283">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440485" alias="SC_EXP_30598_1#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D1, constructed from sample accession ERS3460284 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCGACTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440486" alias="SC_EXP_30598_1#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E1, constructed from sample accession ERS3460285 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATTTATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460285">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440487" alias="SC_EXP_30598_1#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F1, constructed from sample accession ERS3460286 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTAAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460286">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460286</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440488" alias="SC_EXP_30598_1#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G1, constructed from sample accession ERS3460287 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTAGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460287">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460287</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440489" alias="SC_EXP_30598_1#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H1, constructed from sample accession ERS3460288 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460288">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440490" alias="SC_EXP_30598_1#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I1, constructed from sample accession ERS3460289 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTGATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440491" alias="SC_EXP_30598_1#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J1, constructed from sample accession ERS3460290 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCTCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440492" alias="SC_EXP_30598_1#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K1, constructed from sample accession ERS3460291 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TATTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460291">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440493" alias="SC_EXP_30598_1#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L1, constructed from sample accession ERS3460292 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCTCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656267</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440494" alias="SC_EXP_30598_1#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M1, constructed from sample accession ERS3460293 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTACGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440495" alias="SC_EXP_30598_1#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N1, constructed from sample accession ERS3460294 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCGGGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440496" alias="SC_EXP_30598_1#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O1, constructed from sample accession ERS3460295 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440497" alias="SC_EXP_30598_1#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P1, constructed from sample accession ERS3460296 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440498" alias="SC_EXP_30598_1#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A2, constructed from sample accession ERS3460297 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460297">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656272</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440499" alias="SC_EXP_30598_1#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B2, constructed from sample accession ERS3460298 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440500" alias="SC_EXP_30598_1#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C2, constructed from sample accession ERS3460299 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GATACTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440501" alias="SC_EXP_30598_1#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D2, constructed from sample accession ERS3460300 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440502" alias="SC_EXP_30598_1#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E2, constructed from sample accession ERS3460304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCAAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656279</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440503" alias="SC_EXP_30598_1#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F2, constructed from sample accession ERS3460305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTCGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656280</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440504" alias="SC_EXP_30598_1#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G2, constructed from sample accession ERS3460306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCGGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440505" alias="SC_EXP_30598_1#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H2, constructed from sample accession ERS3460307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTCATATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440506" alias="SC_EXP_30598_1#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I2, constructed from sample accession ERS3460308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCTTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440507" alias="SC_EXP_30598_1#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J2, constructed from sample accession ERS3460309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656284</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440508" alias="SC_EXP_30598_1#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K2, constructed from sample accession ERS3460310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCACTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440509" alias="SC_EXP_30598_1#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L2, constructed from sample accession ERS3460311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCGATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440510" alias="SC_EXP_30598_1#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M2, constructed from sample accession ERS3460301 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440511" alias="SC_EXP_30598_1#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N2, constructed from sample accession ERS3460302 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656277</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440512" alias="SC_EXP_30598_1#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O2, constructed from sample accession ERS3460303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440513" alias="SC_EXP_30598_1#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P2, constructed from sample accession ERS3460312 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440514" alias="SC_EXP_30598_1#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A3, constructed from sample accession ERS3460313 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TATATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656288</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440515" alias="SC_EXP_30598_1#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B3, constructed from sample accession ERS3460314 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656289</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440516" alias="SC_EXP_30598_1#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C3, constructed from sample accession ERS3460315 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTATCCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656290</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440517" alias="SC_EXP_30598_1#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D3, constructed from sample accession ERS3460316 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCCACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440518" alias="SC_EXP_30598_1#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E3, constructed from sample accession ERS3460317 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTACCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460317">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656292</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440519" alias="SC_EXP_30598_1#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F3, constructed from sample accession ERS3460318 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCCTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656293</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440520" alias="SC_EXP_30598_1#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G3, constructed from sample accession ERS3460319 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAGAGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440521" alias="SC_EXP_30598_1#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H3, constructed from sample accession ERS3460320 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTCGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656295</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440522" alias="SC_EXP_30598_1#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I3, constructed from sample accession ERS3460321 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656296</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440523" alias="SC_EXP_30598_1#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J3, constructed from sample accession ERS3460322 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGACGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440524" alias="SC_EXP_30598_1#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K3, constructed from sample accession ERS3460323 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTCCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656298</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440525" alias="SC_EXP_30598_1#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L3, constructed from sample accession ERS3460324 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGTGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656299</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440526" alias="SC_EXP_30598_1#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M3, constructed from sample accession ERS3460325 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TAGGCGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440527" alias="SC_EXP_30598_1#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N3, constructed from sample accession ERS3460326 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTCAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656301</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440528" alias="SC_EXP_30598_1#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O3, constructed from sample accession ERS3460327 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GACTTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460327">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656302</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440529" alias="SC_EXP_30598_1#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P3, constructed from sample accession ERS3460328 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACTCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440530" alias="SC_EXP_30598_1#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A4, constructed from sample accession ERS3460329 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGCTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440531" alias="SC_EXP_30598_1#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B4, constructed from sample accession ERS3460330 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GACTATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656305</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440532" alias="SC_EXP_30598_1#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C4, constructed from sample accession ERS3460331 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGTGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440533" alias="SC_EXP_30598_1#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D4, constructed from sample accession ERS3460332 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440534" alias="SC_EXP_30598_1#53">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E4, constructed from sample accession ERS3460333 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACAAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656308</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440535" alias="SC_EXP_30598_1#54">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F4, constructed from sample accession ERS3460334 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656309</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440537" alias="SC_EXP_30598_1#56">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H4, constructed from sample accession ERS3460336 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCGGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440538" alias="SC_EXP_30598_1#57">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I4, constructed from sample accession ERS3460337 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGCGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440540" alias="SC_EXP_30598_1#59">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K4, constructed from sample accession ERS3460339 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCACGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440541" alias="SC_EXP_30598_1#60">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L4, constructed from sample accession ERS3460340 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCTAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656315</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440543" alias="SC_EXP_30598_1#62">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N4, constructed from sample accession ERS3460342 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTCCAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440544" alias="SC_EXP_30598_1#63">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O4, constructed from sample accession ERS3460343 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATGGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656318</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440546" alias="SC_EXP_30598_1#65">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A5, constructed from sample accession ERS3460345 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCATCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440547" alias="SC_EXP_30598_1#66">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B5, constructed from sample accession ERS3460346 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCATGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440549" alias="SC_EXP_30598_1#68">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D5, constructed from sample accession ERS3460348 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCTTGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440550" alias="SC_EXP_30598_1#69">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E5, constructed from sample accession ERS3460349 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTAAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656324</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440552" alias="SC_EXP_30598_1#71">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G5, constructed from sample accession ERS3460351 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440553" alias="SC_EXP_30598_1#72">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H5, constructed from sample accession ERS3460352 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTTCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656327</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440555" alias="SC_EXP_30598_1#74">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J5, constructed from sample accession ERS3460354 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTATATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440556" alias="SC_EXP_30598_1#75">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K5, constructed from sample accession ERS3460355 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCGCTAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440558" alias="SC_EXP_30598_1#77">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M5, constructed from sample accession ERS3460357 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCCACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440559" alias="SC_EXP_30598_1#78">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N5, constructed from sample accession ERS3460358 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCGCCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440561" alias="SC_EXP_30598_1#80">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P5, constructed from sample accession ERS3460360 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTGGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440562" alias="SC_EXP_30598_1#81">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A6, constructed from sample accession ERS3460361 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGATTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656336</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440564" alias="SC_EXP_30598_1#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C6, constructed from sample accession ERS3460363 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AACTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656338</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440565" alias="SC_EXP_30598_1#84">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D6, constructed from sample accession ERS3460364 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCCTATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440567" alias="SC_EXP_30598_1#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F6, constructed from sample accession ERS3460366 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656341</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440568" alias="SC_EXP_30598_1#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G6, constructed from sample accession ERS3460367 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCTCGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656342</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440570" alias="SC_EXP_30598_1#89">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I6, constructed from sample accession ERS3460369 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTCGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440571" alias="SC_EXP_30598_1#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J6, constructed from sample accession ERS3460370 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656345</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440573" alias="SC_EXP_30598_1#92">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L6, constructed from sample accession ERS3460372 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGGGTTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656347</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440574" alias="SC_EXP_30598_1#93">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M6, constructed from sample accession ERS3460373 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGGCTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440576" alias="SC_EXP_30598_1#95">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O6, constructed from sample accession ERS3460375 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCTGTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656350</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440577" alias="SC_EXP_30598_1#96">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P6, constructed from sample accession ERS3460376 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCGTACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440579" alias="SC_EXP_30598_1#98">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B7, constructed from sample accession ERS3460378 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440580" alias="SC_EXP_30598_1#99">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C7, constructed from sample accession ERS3460379 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTGCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440582" alias="SC_EXP_30598_1#101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#101</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E7, constructed from sample accession ERS3460381 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTAGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440583" alias="SC_EXP_30598_1#102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F7, constructed from sample accession ERS3460382 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACGTTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440585" alias="SC_EXP_30598_1#104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H7, constructed from sample accession ERS3460384 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCTTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440586" alias="SC_EXP_30598_1#105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I7, constructed from sample accession ERS3460385 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ATATGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440588" alias="SC_EXP_30598_1#107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K7, constructed from sample accession ERS3460387 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440589" alias="SC_EXP_30598_1#108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L7, constructed from sample accession ERS3460388 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440591" alias="SC_EXP_30598_1#110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N7, constructed from sample accession ERS3460390 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGCATCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440592" alias="SC_EXP_30598_1#111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O7, constructed from sample accession ERS3460391 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGATAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440594" alias="SC_EXP_30598_1#113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#113</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A8, constructed from sample accession ERS3460393 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440595" alias="SC_EXP_30598_1#114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B8, constructed from sample accession ERS3460394 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCATCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440597" alias="SC_EXP_30598_1#116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#116</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D8, constructed from sample accession ERS3460396 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCGGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440598" alias="SC_EXP_30598_1#117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#117</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E8, constructed from sample accession ERS3460397 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAGAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440600" alias="SC_EXP_30598_1#119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#119</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G8, constructed from sample accession ERS3460399 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAAACCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656374</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440601" alias="SC_EXP_30598_1#120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#120</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H8, constructed from sample accession ERS3460400 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440603" alias="SC_EXP_30598_1#122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J8, constructed from sample accession ERS3460402 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460402">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440604" alias="SC_EXP_30598_1#123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K8, constructed from sample accession ERS3460403 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440473" alias="SC_EXP_30501_1#376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30501_1#376</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30501_1#376</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571489T:H24, constructed from sample accession ERS3460272 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30501_1).  This submission includes reads tagged with the sequence CTATACCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656247</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571489T:H24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440536" alias="SC_EXP_30598_1#55">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G4, constructed from sample accession ERS3460335 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTAACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656310</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440539" alias="SC_EXP_30598_1#58">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J4, constructed from sample accession ERS3460338 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCCTGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656313</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440542" alias="SC_EXP_30598_1#61">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M4, constructed from sample accession ERS3460341 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAACCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440545" alias="SC_EXP_30598_1#64">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P4, constructed from sample accession ERS3460344 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GATTAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656319</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440548" alias="SC_EXP_30598_1#67">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C5, constructed from sample accession ERS3460347 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACTTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656322</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440551" alias="SC_EXP_30598_1#70">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F5, constructed from sample accession ERS3460350 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656325</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440554" alias="SC_EXP_30598_1#73">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I5, constructed from sample accession ERS3460353 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTCCGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656328</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440557" alias="SC_EXP_30598_1#76">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L5, constructed from sample accession ERS3460356 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCTAAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440560" alias="SC_EXP_30598_1#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O5, constructed from sample accession ERS3460359 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AACTTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440563" alias="SC_EXP_30598_1#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B6, constructed from sample accession ERS3460362 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACGCCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656337</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440566" alias="SC_EXP_30598_1#85">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E6, constructed from sample accession ERS3460365 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AAACGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440569" alias="SC_EXP_30598_1#88">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H6, constructed from sample accession ERS3460368 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TACGGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440572" alias="SC_EXP_30598_1#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K6, constructed from sample accession ERS3460371 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCACGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656346</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440575" alias="SC_EXP_30598_1#94">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N6, constructed from sample accession ERS3460374 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGATCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440578" alias="SC_EXP_30598_1#97">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#97</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A7, constructed from sample accession ERS3460377 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTAACTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440581" alias="SC_EXP_30598_1#100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D7, constructed from sample accession ERS3460380 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCTGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440584" alias="SC_EXP_30598_1#103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G7, constructed from sample accession ERS3460383 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTGGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440587" alias="SC_EXP_30598_1#106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J7, constructed from sample accession ERS3460386 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGACGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440590" alias="SC_EXP_30598_1#109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M7, constructed from sample accession ERS3460389 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGCCTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440593" alias="SC_EXP_30598_1#112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P7, constructed from sample accession ERS3460392 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460392">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440596" alias="SC_EXP_30598_1#115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C8, constructed from sample accession ERS3460395 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440599" alias="SC_EXP_30598_1#118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#118</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F8, constructed from sample accession ERS3460398 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGCAAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440602" alias="SC_EXP_30598_1#121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#121</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I8, constructed from sample accession ERS3460401 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAGACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440605" alias="SC_EXP_30598_1#124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L8, constructed from sample accession ERS3460404 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCGGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440606" alias="SC_EXP_30598_1#125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#125</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M8, constructed from sample accession ERS3460405 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCCGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460405">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440607" alias="SC_EXP_30598_1#126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#126</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N8, constructed from sample accession ERS3460406 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460406">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440608" alias="SC_EXP_30598_1#127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O8, constructed from sample accession ERS3460407 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460407">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440609" alias="SC_EXP_30598_1#128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P8, constructed from sample accession ERS3460408 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTAGATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440610" alias="SC_EXP_30598_1#129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#129</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A9, constructed from sample accession ERS3460409 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTCGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656384</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440611" alias="SC_EXP_30598_1#130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#130</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B9, constructed from sample accession ERS3460410 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656385</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440612" alias="SC_EXP_30598_1#131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#131</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C9, constructed from sample accession ERS3460411 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656386</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440613" alias="SC_EXP_30598_1#132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D9, constructed from sample accession ERS3460412 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656387</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440614" alias="SC_EXP_30598_1#133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#133</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E9, constructed from sample accession ERS3460413 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCATGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656388</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440615" alias="SC_EXP_30598_1#134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#134</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F9, constructed from sample accession ERS3460414 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTAATCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656389</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440616" alias="SC_EXP_30598_1#135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#135</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G9, constructed from sample accession ERS3460415 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGTACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440617" alias="SC_EXP_30598_1#136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H9, constructed from sample accession ERS3460416 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTATGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656391</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440618" alias="SC_EXP_30598_1#137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#137</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I9, constructed from sample accession ERS3460417 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTAAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656392</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440619" alias="SC_EXP_30598_1#138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#138</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J9, constructed from sample accession ERS3460418 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTATGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440620" alias="SC_EXP_30598_1#139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K9, constructed from sample accession ERS3460419 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440621" alias="SC_EXP_30598_1#140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L9, constructed from sample accession ERS3460420 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGTTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656395</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440622" alias="SC_EXP_30598_1#141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#141</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M9, constructed from sample accession ERS3460421 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GACGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440623" alias="SC_EXP_30598_1#142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#142</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N9, constructed from sample accession ERS3460422 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TATATTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656397</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440624" alias="SC_EXP_30598_1#143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O9, constructed from sample accession ERS3460423 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGCTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656398</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440625" alias="SC_EXP_30598_1#144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P9, constructed from sample accession ERS3460424 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGACCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440626" alias="SC_EXP_30598_1#145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#145</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A10, constructed from sample accession ERS3460425 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTCTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656400</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440627" alias="SC_EXP_30598_1#146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#146</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B10, constructed from sample accession ERS3460426 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCGGGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440628" alias="SC_EXP_30598_1#147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C10, constructed from sample accession ERS3460427 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440629" alias="SC_EXP_30598_1#148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D10, constructed from sample accession ERS3460428 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACGTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440630" alias="SC_EXP_30598_1#149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#149</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E10, constructed from sample accession ERS3460429 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAAACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440631" alias="SC_EXP_30598_1#150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#150</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F10, constructed from sample accession ERS3460430 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGTATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440632" alias="SC_EXP_30598_1#151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#151</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G10, constructed from sample accession ERS3460431 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCCATTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440633" alias="SC_EXP_30598_1#152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H10, constructed from sample accession ERS3460432 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCGTTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656407</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440634" alias="SC_EXP_30598_1#153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#153</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I10, constructed from sample accession ERS3460433 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440635" alias="SC_EXP_30598_1#154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#154</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J10, constructed from sample accession ERS3460434 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGCTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440636" alias="SC_EXP_30598_1#155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K10, constructed from sample accession ERS3460435 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCCAAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440637" alias="SC_EXP_30598_1#156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L10, constructed from sample accession ERS3460436 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTCGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440638" alias="SC_EXP_30598_1#157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#157</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M10, constructed from sample accession ERS3460437 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACTGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440639" alias="SC_EXP_30598_1#158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#158</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N10, constructed from sample accession ERS3460438 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440640" alias="SC_EXP_30598_1#159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#159</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O10, constructed from sample accession ERS3460439 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAGGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440641" alias="SC_EXP_30598_1#160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P10, constructed from sample accession ERS3460440 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AACCAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440642" alias="SC_EXP_30598_1#161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#161</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A11, constructed from sample accession ERS3460441 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460441">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440643" alias="SC_EXP_30598_1#162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#162</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B11, constructed from sample accession ERS3460442 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656417</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440644" alias="SC_EXP_30598_1#163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C11, constructed from sample accession ERS3460443 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460443">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440645" alias="SC_EXP_30598_1#164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D11, constructed from sample accession ERS3460444 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTGGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460444">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440646" alias="SC_EXP_30598_1#165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440646</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#165</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E11, constructed from sample accession ERS3460445 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GATATGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440647" alias="SC_EXP_30598_1#166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#166</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F11, constructed from sample accession ERS3460446 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCGAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460446">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656421</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440648" alias="SC_EXP_30598_1#167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440648</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#167</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G11, constructed from sample accession ERS3460447 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460447">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440649" alias="SC_EXP_30598_1#168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440649</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H11, constructed from sample accession ERS3460448 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTCGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460448">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440650" alias="SC_EXP_30598_1#169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440650</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#169</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I11, constructed from sample accession ERS3460449 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460449">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440651" alias="SC_EXP_30598_1#170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440651</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#170</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J11, constructed from sample accession ERS3460450 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ATCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656425</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440652" alias="SC_EXP_30598_1#171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440652</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K11, constructed from sample accession ERS3460451 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440653" alias="SC_EXP_30598_1#172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440653</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#172</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L11, constructed from sample accession ERS3460452 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGGGCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440654" alias="SC_EXP_30598_1#173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440654</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#173</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M11, constructed from sample accession ERS3460453 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCGGCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460453">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440655" alias="SC_EXP_30598_1#174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440655</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#174</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N11, constructed from sample accession ERS3460454 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGCACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460454">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440656" alias="SC_EXP_30598_1#175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440656</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O11, constructed from sample accession ERS3460455 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440657" alias="SC_EXP_30598_1#176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440657</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P11, constructed from sample accession ERS3460456 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAAATAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440658" alias="SC_EXP_30598_1#177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440658</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#177</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A12, constructed from sample accession ERS3460457 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440659" alias="SC_EXP_30598_1#178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440659</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#178</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B12, constructed from sample accession ERS3460458 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440660" alias="SC_EXP_30598_1#179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440660</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#179</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C12, constructed from sample accession ERS3460459 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAAAGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460459">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440661" alias="SC_EXP_30598_1#180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D12, constructed from sample accession ERS3460460 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCAAAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460460">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440662" alias="SC_EXP_30598_1#181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440662</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#181</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E12, constructed from sample accession ERS3460461 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGACGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460461">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460461</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440663" alias="SC_EXP_30598_1#182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440663</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#182</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F12, constructed from sample accession ERS3460462 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCTTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460462">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440664" alias="SC_EXP_30598_1#183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#183</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G12, constructed from sample accession ERS3460463 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGAAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460463">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440665" alias="SC_EXP_30598_1#184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#184</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H12, constructed from sample accession ERS3460464 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAGGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460464">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440666" alias="SC_EXP_30598_1#185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#185</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I12, constructed from sample accession ERS3460465 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460465">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440667" alias="SC_EXP_30598_1#186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440667</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#186</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J12, constructed from sample accession ERS3460466 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCGGGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460466">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656441</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440668" alias="SC_EXP_30598_1#187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440668</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#187</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K12, constructed from sample accession ERS3460467 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGTTGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460467">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440669" alias="SC_EXP_30598_1#188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440669</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#188</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L12, constructed from sample accession ERS3460468 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460468">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440670" alias="SC_EXP_30598_1#189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440670</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#189</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M12, constructed from sample accession ERS3460469 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCCTTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460469">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440671" alias="SC_EXP_30598_1#190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440671</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#190</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N12, constructed from sample accession ERS3460470 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCCGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460470">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460470</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656445</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440672" alias="SC_EXP_30598_1#191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440672</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#191</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O12, constructed from sample accession ERS3460471 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAGAAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460471">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460471</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656446</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440673" alias="SC_EXP_30598_1#192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#192</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P12, constructed from sample accession ERS3460472 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAAATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460472">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440674" alias="SC_EXP_30598_1#193">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#193</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#193</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A13, constructed from sample accession ERS3460473 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTACCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460473">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440675" alias="SC_EXP_30598_1#194">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#194</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B13, constructed from sample accession ERS3460474 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTTCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460474">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440676" alias="SC_EXP_30598_1#195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#195</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C13, constructed from sample accession ERS3460475 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TACGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460475">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460475</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656450</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440677" alias="SC_EXP_30598_1#196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#196</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D13, constructed from sample accession ERS3460476 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460476">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460476</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440678" alias="SC_EXP_30598_1#197">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#197</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E13, constructed from sample accession ERS3460477 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTCGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460477">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460477</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440679" alias="SC_EXP_30598_1#198">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#198</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F13, constructed from sample accession ERS3460478 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AATAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440680" alias="SC_EXP_30598_1#199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#199</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G13, constructed from sample accession ERS3460479 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCACTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460479">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460479</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440681" alias="SC_EXP_30598_1#200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#200</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H13, constructed from sample accession ERS3460480 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460480">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460480</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440682" alias="SC_EXP_30598_1#201">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#201</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I13, constructed from sample accession ERS3460481 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGATGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460481">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460481</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440683" alias="SC_EXP_30598_1#202">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#202</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#202</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J13, constructed from sample accession ERS3460482 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCGTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460482">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460482</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440684" alias="SC_EXP_30598_1#203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#203</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K13, constructed from sample accession ERS3460483 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460483">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460483</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440685" alias="SC_EXP_30598_1#204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#204</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L13, constructed from sample accession ERS3460484 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGACTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460484">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460484</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440686" alias="SC_EXP_30598_1#205">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#205</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#205</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M13, constructed from sample accession ERS3460485 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TAGTATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460485">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460485</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440687" alias="SC_EXP_30598_1#206">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#206</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N13, constructed from sample accession ERS3460486 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGGGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460486">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460486</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440688" alias="SC_EXP_30598_1#207">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#207</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O13, constructed from sample accession ERS3460487 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGACACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460487">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460487</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440689" alias="SC_EXP_30598_1#208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#208</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P13, constructed from sample accession ERS3460488 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GATATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460488">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460488</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440690" alias="SC_EXP_30598_1#209">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#209</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A14, constructed from sample accession ERS3460489 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460489">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460489</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440691" alias="SC_EXP_30598_1#210">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#210</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B14, constructed from sample accession ERS3460490 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460490">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460490</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440692" alias="SC_EXP_30598_1#211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#211</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C14, constructed from sample accession ERS3460491 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTTGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460491">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460491</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440693" alias="SC_EXP_30598_1#212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#212</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D14, constructed from sample accession ERS3460492 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460492">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460492</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440694" alias="SC_EXP_30598_1#213">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#213</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#213</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E14, constructed from sample accession ERS3460493 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGGGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460493">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440695" alias="SC_EXP_30598_1#214">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#214</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F14, constructed from sample accession ERS3460494 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCGGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460494">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460494</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440696" alias="SC_EXP_30598_1#215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#215</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G14, constructed from sample accession ERS3460495 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GACGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460495">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460495</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440697" alias="SC_EXP_30598_1#216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#216</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H14, constructed from sample accession ERS3460496 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCGGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460496">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460496</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440698" alias="SC_EXP_30598_1#217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#217</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I14, constructed from sample accession ERS3460497 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCTTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460497">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460497</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440699" alias="SC_EXP_30598_1#218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#218</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J14, constructed from sample accession ERS3460498 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460498">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460498</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440700" alias="SC_EXP_30598_1#219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#219</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K14, constructed from sample accession ERS3460499 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTTCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460499">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460499</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440701" alias="SC_EXP_30598_1#220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#220</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L14, constructed from sample accession ERS3460500 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AACGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460500">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460500</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440702" alias="SC_EXP_30598_1#221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#221</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M14, constructed from sample accession ERS3460501 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGCACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460501">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460501</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440703" alias="SC_EXP_30598_1#222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#222</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#222</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N14, constructed from sample accession ERS3460502 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460502">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460502</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440704" alias="SC_EXP_30598_1#223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#223</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O14, constructed from sample accession ERS3460503 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460503">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460503</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440705" alias="SC_EXP_30598_1#224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#224</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P14, constructed from sample accession ERS3460504 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460504">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460504</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440706" alias="SC_EXP_30598_1#225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#225</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A15, constructed from sample accession ERS3460505 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGTAGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460505">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460505</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440707" alias="SC_EXP_30598_1#226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#226</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#226</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B15, constructed from sample accession ERS3460506 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AATGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460506">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460506</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440708" alias="SC_EXP_30598_1#227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#227</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C15, constructed from sample accession ERS3460507 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460507">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460507</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440709" alias="SC_EXP_30598_1#228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#228</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D15, constructed from sample accession ERS3460508 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCAATAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460508">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460508</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440710" alias="SC_EXP_30598_1#229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#229</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E15, constructed from sample accession ERS3460509 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTGTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460509">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460509</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440711" alias="SC_EXP_30598_1#230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#230</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F15, constructed from sample accession ERS3460510 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460510">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460510</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440712" alias="SC_EXP_30598_1#231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#231</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#231</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G15, constructed from sample accession ERS3460511 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460511">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460511</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440713" alias="SC_EXP_30598_1#232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#232</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H15, constructed from sample accession ERS3460512 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440714" alias="SC_EXP_30598_1#233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#233</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I15, constructed from sample accession ERS3460513 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTGCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460513">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440715" alias="SC_EXP_30598_1#234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#234</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J15, constructed from sample accession ERS3460514 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCGCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460514">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440716" alias="SC_EXP_30598_1#235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#235</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K15, constructed from sample accession ERS3460515 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATATTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460515">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460515</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440717" alias="SC_EXP_30598_1#236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#236</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L15, constructed from sample accession ERS3460516 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCAAACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460516">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460516</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440718" alias="SC_EXP_30598_1#237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#237</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M15, constructed from sample accession ERS3460517 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCCTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460517">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440719" alias="SC_EXP_30598_1#238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#238</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N15, constructed from sample accession ERS3460518 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCGATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460518">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656493</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440720" alias="SC_EXP_30598_1#239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#239</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O15, constructed from sample accession ERS3460519 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GACTCCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460519">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440721" alias="SC_EXP_30598_1#240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#240</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P15, constructed from sample accession ERS3460520 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460520">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460520</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440722" alias="SC_EXP_30598_1#241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#241</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A16, constructed from sample accession ERS3460521 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460521">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460521</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440723" alias="SC_EXP_30598_1#242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#242</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#242</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B16, constructed from sample accession ERS3460522 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCTTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460522">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460522</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440724" alias="SC_EXP_30598_1#243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#243</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#243</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C16, constructed from sample accession ERS3460523 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTCACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460523">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460523</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656498</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440725" alias="SC_EXP_30598_1#244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#244</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#244</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D16, constructed from sample accession ERS3460524 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGGCCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460524">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460524</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440726" alias="SC_EXP_30598_1#245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#245</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E16, constructed from sample accession ERS3460525 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGGCTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460525">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460525</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440727" alias="SC_EXP_30598_1#246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#246</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F16, constructed from sample accession ERS3460526 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCTGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460526">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460526</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440728" alias="SC_EXP_30598_1#247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#247</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G16, constructed from sample accession ERS3460527 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCTCTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460527">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460527</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440729" alias="SC_EXP_30598_1#248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#248</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H16, constructed from sample accession ERS3460528 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCGGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460528">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460528</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440730" alias="SC_EXP_30598_1#249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#249</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I16, constructed from sample accession ERS3460529 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460529">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460529</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440731" alias="SC_EXP_30598_1#250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#250</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J16, constructed from sample accession ERS3460530 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460530">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460530</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440732" alias="SC_EXP_30598_1#251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#251</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K16, constructed from sample accession ERS3460531 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCGCATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460531">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460531</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440733" alias="SC_EXP_30598_1#252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#252</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L16, constructed from sample accession ERS3460532 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGACGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460532">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460532</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440734" alias="SC_EXP_30598_1#253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#253</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M16, constructed from sample accession ERS3460533 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460533">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460533</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440735" alias="SC_EXP_30598_1#254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#254</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N16, constructed from sample accession ERS3460534 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTAAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460534">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460534</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440736" alias="SC_EXP_30598_1#255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#255</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O16, constructed from sample accession ERS3460535 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTCTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460535">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460535</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656510</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440737" alias="SC_EXP_30598_1#256">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#256</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#256</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P16, constructed from sample accession ERS3460536 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTTCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460536">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460536</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656511</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440738" alias="SC_EXP_30598_1#257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#257</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A17, constructed from sample accession ERS3460537 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCACGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460537">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460537</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440739" alias="SC_EXP_30598_1#258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#258</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B17, constructed from sample accession ERS3460538 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460538">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460538</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440740" alias="SC_EXP_30598_1#259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#259</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C17, constructed from sample accession ERS3460539 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCTGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460539">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460539</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656514</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440741" alias="SC_EXP_30598_1#260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#260</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D17, constructed from sample accession ERS3460540 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCTGAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460540">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460540</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440742" alias="SC_EXP_30598_1#261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#261</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E17, constructed from sample accession ERS3460541 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCAGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460541">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460541</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656516</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440743" alias="SC_EXP_30598_1#262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#262</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#262</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F17, constructed from sample accession ERS3460542 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGAAAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460542">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460542</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656517</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440744" alias="SC_EXP_30598_1#263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#263</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#263</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G17, constructed from sample accession ERS3460543 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460543">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460543</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440745" alias="SC_EXP_30598_1#264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#264</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#264</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H17, constructed from sample accession ERS3460544 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGGTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460544">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460544</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440746" alias="SC_EXP_30598_1#265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#265</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#265</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I17, constructed from sample accession ERS3460545 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460545">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460545</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440747" alias="SC_EXP_30598_1#266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#266</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#266</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J17, constructed from sample accession ERS3460546 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460546">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460546</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440748" alias="SC_EXP_30598_1#267">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#267</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#267</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K17, constructed from sample accession ERS3460547 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TATCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460547">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460547</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440749" alias="SC_EXP_30598_1#268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#268</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#268</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L17, constructed from sample accession ERS3460548 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCAGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460548">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460548</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440750" alias="SC_EXP_30598_1#269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#269</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M17, constructed from sample accession ERS3460549 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACTGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460549">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460549</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440751" alias="SC_EXP_30598_1#270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#270</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#270</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N17, constructed from sample accession ERS3460550 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGGGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460550">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460550</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440752" alias="SC_EXP_30598_1#271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#271</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#271</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O17, constructed from sample accession ERS3460551 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGAGTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460551">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460551</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440753" alias="SC_EXP_30598_1#272">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#272</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#272</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P17, constructed from sample accession ERS3460552 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460552">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460552</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440754" alias="SC_EXP_30598_1#273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#273</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A18, constructed from sample accession ERS3460553 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGGCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460553">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460553</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440755" alias="SC_EXP_30598_1#274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#274</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#274</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B18, constructed from sample accession ERS3460554 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTGAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460554">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460554</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440756" alias="SC_EXP_30598_1#275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#275</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#275</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C18, constructed from sample accession ERS3460555 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCGCTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460555">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460555</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440757" alias="SC_EXP_30598_1#276">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#276</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#276</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D18, constructed from sample accession ERS3460562 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCCTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460562">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460562</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656537</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440758" alias="SC_EXP_30598_1#277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#277</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#277</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E18, constructed from sample accession ERS3460563 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTGCGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460563">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460563</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656538</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440759" alias="SC_EXP_30598_1#278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#278</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#278</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F18, constructed from sample accession ERS3460564 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AAAGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460564">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460564</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656539</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440760" alias="SC_EXP_30598_1#279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#279</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#279</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G18, constructed from sample accession ERS3460565 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCCGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460565">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460565</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656540</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440761" alias="SC_EXP_30598_1#280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#280</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#280</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H18, constructed from sample accession ERS3460566 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACTCGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460566">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460566</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656541</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440762" alias="SC_EXP_30598_1#281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#281</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I18, constructed from sample accession ERS3460567 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AACCGGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460567">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460567</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656542</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440763" alias="SC_EXP_30598_1#282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#282</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#282</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J18, constructed from sample accession ERS3460568 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGATTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460568">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460568</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656543</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440764" alias="SC_EXP_30598_1#283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#283</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#283</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K18, constructed from sample accession ERS3460569 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460569">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460569</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656544</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440765" alias="SC_EXP_30598_1#284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#284</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#284</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L18, constructed from sample accession ERS3460556 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTAAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460556">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460556</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656531</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440766" alias="SC_EXP_30598_1#285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#285</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M18, constructed from sample accession ERS3460557 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCTAGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460557">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460557</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440767" alias="SC_EXP_30598_1#286">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#286</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#286</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N18, constructed from sample accession ERS3460558 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCTTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460558">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460558</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440768" alias="SC_EXP_30598_1#287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#287</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#287</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O18, constructed from sample accession ERS3460559 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTATTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460559">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460559</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440769" alias="SC_EXP_30598_1#288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#288</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#288</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P18, constructed from sample accession ERS3460560 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460560">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460560</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440770" alias="SC_EXP_30598_1#289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#289</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#289</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A19, constructed from sample accession ERS3460561 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCGGAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460561">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460561</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440771" alias="SC_EXP_30598_1#290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#290</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#290</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B19, constructed from sample accession ERS3460570 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTGACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460570">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460570</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656545</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440772" alias="SC_EXP_30598_1#291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#291</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#291</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C19, constructed from sample accession ERS3460571 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTGGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460571">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460571</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656546</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440773" alias="SC_EXP_30598_1#292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#292</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#292</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D19, constructed from sample accession ERS3460572 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460572">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460572</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656547</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440774" alias="SC_EXP_30598_1#293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#293</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E19, constructed from sample accession ERS3460573 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTCAAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460573">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460573</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440775" alias="SC_EXP_30598_1#294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#294</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F19, constructed from sample accession ERS3460574 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460574">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460574</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440776" alias="SC_EXP_30598_1#295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#295</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G19, constructed from sample accession ERS3460575 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460575">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460575</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440777" alias="SC_EXP_30598_1#296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#296</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H19, constructed from sample accession ERS3460576 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460576">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460576</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440778" alias="SC_EXP_30598_1#297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#297</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I19, constructed from sample accession ERS3460577 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCTAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460577">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460577</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440779" alias="SC_EXP_30598_1#298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J19, constructed from sample accession ERS3460578 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCGTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460578">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460578</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440780" alias="SC_EXP_30598_1#299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K19, constructed from sample accession ERS3460579 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGAGGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460579">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460579</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440781" alias="SC_EXP_30598_1#300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L19, constructed from sample accession ERS3460580 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTAGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460580">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460580</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656555</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440782" alias="SC_EXP_30598_1#301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M19, constructed from sample accession ERS3460581 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGCGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460581">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460581</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656556</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440783" alias="SC_EXP_30598_1#302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N19, constructed from sample accession ERS3460582 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACGCGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460582">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460582</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656557</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440784" alias="SC_EXP_30598_1#303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#303</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O19, constructed from sample accession ERS3460583 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCGCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460583">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460583</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656558</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440785" alias="SC_EXP_30598_1#304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#304</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P19, constructed from sample accession ERS3460584 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460584">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460584</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656559</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440786" alias="SC_EXP_30598_1#305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#305</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A20, constructed from sample accession ERS3460585 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGTGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460585">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460585</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656560</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440787" alias="SC_EXP_30598_1#306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#306</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B20, constructed from sample accession ERS3460586 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460586">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460586</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656561</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440788" alias="SC_EXP_30598_1#307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#307</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C20, constructed from sample accession ERS3460587 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460587">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460587</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656562</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440789" alias="SC_EXP_30598_1#308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D20, constructed from sample accession ERS3460588 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460588">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460588</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656563</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440790" alias="SC_EXP_30598_1#309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E20, constructed from sample accession ERS3460589 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCAAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460589">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460589</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656564</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440791" alias="SC_EXP_30598_1#310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F20, constructed from sample accession ERS3460590 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence ACGTAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460590">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460590</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656565</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440792" alias="SC_EXP_30598_1#311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G20, constructed from sample accession ERS3460591 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCTATATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460591">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460591</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656566</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440793" alias="SC_EXP_30598_1#312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H20, constructed from sample accession ERS3460592 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTTCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460592">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460592</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440794" alias="SC_EXP_30598_1#313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I20, constructed from sample accession ERS3460593 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCTGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460593">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460593</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440795" alias="SC_EXP_30598_1#314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J20, constructed from sample accession ERS3460594 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGACCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460594">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460594</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440796" alias="SC_EXP_30598_1#315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#315</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K20, constructed from sample accession ERS3460595 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGTATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460595">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460595</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656570</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440797" alias="SC_EXP_30598_1#316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#316</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L20, constructed from sample accession ERS3460596 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460596">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460596</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440798" alias="SC_EXP_30598_1#317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#317</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M20, constructed from sample accession ERS3460597 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460597">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460597</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656572</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440799" alias="SC_EXP_30598_1#318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#318</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#318</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N20, constructed from sample accession ERS3460598 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGCAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460598">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460598</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656573</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440800" alias="SC_EXP_30598_1#319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O20, constructed from sample accession ERS3460599 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGGATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460599">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460599</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656574</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440801" alias="SC_EXP_30598_1#320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P20, constructed from sample accession ERS3460600 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGCGGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460600">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460600</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656575</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440802" alias="SC_EXP_30598_1#321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A21, constructed from sample accession ERS3460601 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460601">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460601</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656576</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440803" alias="SC_EXP_30598_1#322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B21, constructed from sample accession ERS3460602 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTTGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460602">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460602</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656577</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440804" alias="SC_EXP_30598_1#323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C21, constructed from sample accession ERS3460603 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCAGGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460603">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460603</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656578</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440805" alias="SC_EXP_30598_1#324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#324</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D21, constructed from sample accession ERS3460604 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460604">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460604</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656579</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440806" alias="SC_EXP_30598_1#325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#325</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E21, constructed from sample accession ERS3460605 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTGTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460605">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460605</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656580</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440807" alias="SC_EXP_30598_1#326">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#326</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#326</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F21, constructed from sample accession ERS3460606 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTTAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460606">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460606</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656581</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440808" alias="SC_EXP_30598_1#327">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#327</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#327</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G21, constructed from sample accession ERS3460607 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AAGGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460607">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460607</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656582</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440809" alias="SC_EXP_30598_1#328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#328</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#328</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H21, constructed from sample accession ERS3460608 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460608">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460608</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656583</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440810" alias="SC_EXP_30598_1#329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#329</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#329</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I21, constructed from sample accession ERS3460609 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTACTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460609">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460609</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656584</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440811" alias="SC_EXP_30598_1#330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#330</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#330</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J21, constructed from sample accession ERS3460610 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCACGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460610">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460610</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440812" alias="SC_EXP_30598_1#331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#331</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#331</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K21, constructed from sample accession ERS3460611 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCGAATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460611">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460611</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656586</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440813" alias="SC_EXP_30598_1#332">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#332</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#332</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L21, constructed from sample accession ERS3460612 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GATGAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460612">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460612</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656587</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440814" alias="SC_EXP_30598_1#333">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#333</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#333</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M21, constructed from sample accession ERS3460613 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTTTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460613">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460613</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440815" alias="SC_EXP_30598_1#334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#334</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#334</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N21, constructed from sample accession ERS3460614 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460614">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460614</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440816" alias="SC_EXP_30598_1#335">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#335</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#335</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O21, constructed from sample accession ERS3460615 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460615">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460615</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440817" alias="SC_EXP_30598_1#336">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#336</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#336</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P21, constructed from sample accession ERS3460616 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AACCTGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460616">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460616</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440818" alias="SC_EXP_30598_1#337">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#337</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#337</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A22, constructed from sample accession ERS3460617 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTTTCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460617">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460617</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440819" alias="SC_EXP_30598_1#338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440819</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#338</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#338</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B22, constructed from sample accession ERS3460618 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AAATGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460618">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460618</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656593</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440820" alias="SC_EXP_30598_1#339">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440820</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#339</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#339</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C22, constructed from sample accession ERS3460619 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CATCGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460619">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460619</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440821" alias="SC_EXP_30598_1#340">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440821</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#340</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#340</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D22, constructed from sample accession ERS3460620 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCACAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460620">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460620</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440822" alias="SC_EXP_30598_1#341">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440822</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#341</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#341</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E22, constructed from sample accession ERS3460621 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AGACTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460621">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460621</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440823" alias="SC_EXP_30598_1#342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440823</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#342</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#342</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F22, constructed from sample accession ERS3460622 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AATGCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460622">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460622</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440824" alias="SC_EXP_30598_1#343">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440824</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#343</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#343</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G22, constructed from sample accession ERS3460623 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GACGGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460623">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460623</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440825" alias="SC_EXP_30598_1#344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440825</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#344</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#344</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H22, constructed from sample accession ERS3460624 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGATAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460624">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460624</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440826" alias="SC_EXP_30598_1#345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440826</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#345</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#345</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I22, constructed from sample accession ERS3460625 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TAGGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460625">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460625</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440827" alias="SC_EXP_30598_1#346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#346</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#346</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J22, constructed from sample accession ERS3460626 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GAGCATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460626">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460626</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440828" alias="SC_EXP_30598_1#347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440828</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#347</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#347</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K22, constructed from sample accession ERS3460627 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460627">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460627</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440829" alias="SC_EXP_30598_1#348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#348</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#348</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L22, constructed from sample accession ERS3460628 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTCTTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460628">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460628</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440830" alias="SC_EXP_30598_1#349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440830</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#349</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#349</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M22, constructed from sample accession ERS3460629 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTAGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460629">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460629</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656604</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440831" alias="SC_EXP_30598_1#350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440831</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#350</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#350</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N22, constructed from sample accession ERS3460630 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGCCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460630">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460630</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440832" alias="SC_EXP_30598_1#351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440832</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#351</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#351</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O22, constructed from sample accession ERS3460631 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGGAGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460631">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460631</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656606</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440833" alias="SC_EXP_30598_1#352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440833</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#352</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#352</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P22, constructed from sample accession ERS3460632 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460632">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656607</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440834" alias="SC_EXP_30598_1#353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440834</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#353</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#353</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A23, constructed from sample accession ERS3460633 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTGAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460633">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440835" alias="SC_EXP_30598_1#354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440835</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#354</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#354</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B23, constructed from sample accession ERS3460634 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTTAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460634">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656609</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440836" alias="SC_EXP_30598_1#355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440836</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#355</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#355</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C23, constructed from sample accession ERS3460635 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTTGGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460635">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460635</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656610</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440837" alias="SC_EXP_30598_1#356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440837</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#356</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#356</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D23, constructed from sample accession ERS3460636 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460636">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440838" alias="SC_EXP_30598_1#357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440838</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#357</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#357</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E23, constructed from sample accession ERS3460637 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AACAGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460637">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656612</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440839" alias="SC_EXP_30598_1#358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440839</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#358</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#358</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F23, constructed from sample accession ERS3460638 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTTGTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460638">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460638</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440840" alias="SC_EXP_30598_1#359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440840</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#359</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#359</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G23, constructed from sample accession ERS3460639 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AATTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460639">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460639</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656614</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440841" alias="SC_EXP_30598_1#360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440841</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#360</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#360</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H23, constructed from sample accession ERS3460640 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence AAAGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460640">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460640</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656615</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440842" alias="SC_EXP_30598_1#361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440842</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#361</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#361</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I23, constructed from sample accession ERS3460641 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGCATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460641">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460641</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440843" alias="SC_EXP_30598_1#362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#362</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#362</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J23, constructed from sample accession ERS3460642 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TCAGTTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460642">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460642</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656617</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440844" alias="SC_EXP_30598_1#363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440844</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#363</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#363</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K23, constructed from sample accession ERS3460643 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGTTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460643">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460643</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656618</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440845" alias="SC_EXP_30598_1#364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440845</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#364</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#364</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L23, constructed from sample accession ERS3460644 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460644">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460644</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656619</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440846" alias="SC_EXP_30598_1#365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440846</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#365</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#365</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M23, constructed from sample accession ERS3460645 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGGGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460645">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460645</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440847" alias="SC_EXP_30598_1#366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#366</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#366</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N23, constructed from sample accession ERS3460646 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCAGCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460646">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656621</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440848" alias="SC_EXP_30598_1#367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440848</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#367</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#367</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O23, constructed from sample accession ERS3460647 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGTGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460647">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656622</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440849" alias="SC_EXP_30598_1#368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440849</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#368</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#368</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P23, constructed from sample accession ERS3460648 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGCCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460648">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440850" alias="SC_EXP_30598_1#369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440850</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#369</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#369</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:A24, constructed from sample accession ERS3460649 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGCACCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460649">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656624</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440851" alias="SC_EXP_30598_1#370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440851</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#370</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#370</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:B24, constructed from sample accession ERS3460650 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CCGATCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460650">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:B24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440852" alias="SC_EXP_30598_1#371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440852</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#371</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#371</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:C24, constructed from sample accession ERS3460651 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CAAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460651">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440853" alias="SC_EXP_30598_1#372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440853</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#372</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#372</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:D24, constructed from sample accession ERS3460652 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GGCGTCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460652">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:D24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440854" alias="SC_EXP_30598_1#373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440854</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#373</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#373</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:E24, constructed from sample accession ERS3460653 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTAGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460653">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440855" alias="SC_EXP_30598_1#374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#374</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#374</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:F24, constructed from sample accession ERS3460654 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GTCGGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460654">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460654</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:F24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440856" alias="SC_EXP_30598_1#375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#375</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#375</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:G24, constructed from sample accession ERS3460655 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCCTCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460655">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460655</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440857" alias="SC_EXP_30598_1#376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#376</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#376</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:H24, constructed from sample accession ERS3460656 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTATACCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460656">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460656</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:H24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440858" alias="SC_EXP_30598_1#377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#377</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#377</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:I24, constructed from sample accession ERS3460657 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TGGTCGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460657">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460657</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440859" alias="SC_EXP_30598_1#378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#378</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#378</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:J24, constructed from sample accession ERS3460658 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTAAACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460658">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460658</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:J24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440860" alias="SC_EXP_30598_1#379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#379</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#379</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:K24, constructed from sample accession ERS3460659 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CGTTGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460659">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460659</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440861" alias="SC_EXP_30598_1#380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440861</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#380</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#380</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:L24, constructed from sample accession ERS3460660 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CACTCTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460660">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460660</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:L24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440027" alias="SC_EXP_30328_3#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552365I, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence CTAAACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552365I</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440028" alias="SC_EXP_30328_3#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552366J, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence TCGGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552366J</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440029" alias="SC_EXP_30328_3#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30328_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30328_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library NT1552367K, constructed from sample accession ERS3535303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30328_3).  This submission includes reads tagged with the sequence AACCGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3535303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3535303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5732000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NT1552367K</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium single cell</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440862" alias="SC_EXP_30598_1#381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#381</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#381</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:M24, constructed from sample accession ERS3460661 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TTGTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460661">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460661</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440863" alias="SC_EXP_30598_1#382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440863</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#382</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#382</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:N24, constructed from sample accession ERS3460662 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence GCAGCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460662">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460662</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:N24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440864" alias="SC_EXP_30598_1#383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440864</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#383</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#383</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:O24, constructed from sample accession ERS3460663 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence CTGCCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460663">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460663</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440865" alias="SC_EXP_30598_1#384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440865</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_1#384</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_1#384</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571384L:P24, constructed from sample accession ERS3460664 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_1).  This submission includes reads tagged with the sequence TACCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460664">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460664</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571384L:P24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440866" alias="SC_EXP_30598_2#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440866</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A1, constructed from sample accession ERS3460665 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460665">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460665</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440867" alias="SC_EXP_30598_2#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440867</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B1, constructed from sample accession ERS3460666 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCGTTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460666">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460666</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440868" alias="SC_EXP_30598_2#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440868</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C1, constructed from sample accession ERS3460667 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTAACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460667">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460667</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440869" alias="SC_EXP_30598_2#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440869</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D1, constructed from sample accession ERS3460668 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCGACTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460668">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460668</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440870" alias="SC_EXP_30598_2#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440870</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E1, constructed from sample accession ERS3460669 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATTTATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460669">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460669</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440871" alias="SC_EXP_30598_2#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440871</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F1, constructed from sample accession ERS3460670 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTAAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460670">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460670</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440872" alias="SC_EXP_30598_2#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440872</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G1, constructed from sample accession ERS3460671 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTAGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460671">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460671</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440873" alias="SC_EXP_30598_2#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440873</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H1, constructed from sample accession ERS3460672 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460672">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460672</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440874" alias="SC_EXP_30598_2#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440874</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I1, constructed from sample accession ERS3460673 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTGATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460673">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460673</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656648</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440875" alias="SC_EXP_30598_2#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440875</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J1, constructed from sample accession ERS3460674 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCTCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460674">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460674</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656649</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440876" alias="SC_EXP_30598_2#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440876</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K1, constructed from sample accession ERS3460675 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TATTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460675">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460675</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440877" alias="SC_EXP_30598_2#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440877</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L1, constructed from sample accession ERS3460676 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCTCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460676">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460676</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440878" alias="SC_EXP_30598_2#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M1, constructed from sample accession ERS3460677 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTACGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460677">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460677</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440879" alias="SC_EXP_30598_2#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N1, constructed from sample accession ERS3460678 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCGGGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460678">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460678</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656653</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440880" alias="SC_EXP_30598_2#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440880</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O1, constructed from sample accession ERS3460679 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460679">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656654</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440881" alias="SC_EXP_30598_2#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440881</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P1, constructed from sample accession ERS3460680 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460680">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440882" alias="SC_EXP_30598_2#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440882</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A2, constructed from sample accession ERS3460681 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460681">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656656</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440883" alias="SC_EXP_30598_2#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440883</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B2, constructed from sample accession ERS3460682 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460682">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656657</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440884" alias="SC_EXP_30598_2#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440884</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C2, constructed from sample accession ERS3460683 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GATACTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460683">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440885" alias="SC_EXP_30598_2#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440885</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D2, constructed from sample accession ERS3460684 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460684">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460684</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440886" alias="SC_EXP_30598_2#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440886</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E2, constructed from sample accession ERS3460685 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCAAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460685">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440887" alias="SC_EXP_30598_2#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440887</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F2, constructed from sample accession ERS3460686 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTCGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460686">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460686</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440888" alias="SC_EXP_30598_2#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440888</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G2, constructed from sample accession ERS3460687 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCGGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460687">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460687</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440889" alias="SC_EXP_30598_2#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440889</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H2, constructed from sample accession ERS3460688 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTCATATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460688">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460688</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656663</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440890" alias="SC_EXP_30598_2#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440890</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I2, constructed from sample accession ERS3460689 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCTTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460689">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460689</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656664</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440891" alias="SC_EXP_30598_2#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440891</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J2, constructed from sample accession ERS3460690 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460690">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460690</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656665</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440892" alias="SC_EXP_30598_2#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440892</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K2, constructed from sample accession ERS3460691 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCACTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460691">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460691</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656666</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440893" alias="SC_EXP_30598_2#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440893</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L2, constructed from sample accession ERS3460692 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCGATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460692">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460692</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656667</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440894" alias="SC_EXP_30598_2#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440894</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M2, constructed from sample accession ERS3460693 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460693">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460693</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440895" alias="SC_EXP_30598_2#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440895</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N2, constructed from sample accession ERS3460694 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460694">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460694</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440896" alias="SC_EXP_30598_2#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440896</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O2, constructed from sample accession ERS3460695 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460695">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460695</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440897" alias="SC_EXP_30598_2#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440897</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P2, constructed from sample accession ERS3460696 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460696">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460696</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656671</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440898" alias="SC_EXP_30598_2#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440898</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A3, constructed from sample accession ERS3460697 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TATATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460697">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460697</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440899" alias="SC_EXP_30598_2#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440899</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B3, constructed from sample accession ERS3460698 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460698">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460698</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440900" alias="SC_EXP_30598_2#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440900</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C3, constructed from sample accession ERS3460699 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTATCCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460699">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460699</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440901" alias="SC_EXP_30598_2#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440901</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D3, constructed from sample accession ERS3460700 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCCACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460700">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460700</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440902" alias="SC_EXP_30598_2#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440902</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E3, constructed from sample accession ERS3460701 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTACCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460701">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460701</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656676</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440903" alias="SC_EXP_30598_2#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440903</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F3, constructed from sample accession ERS3460702 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCCTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460702">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460702</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440904" alias="SC_EXP_30598_2#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440904</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G3, constructed from sample accession ERS3460703 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAGAGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460703">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460703</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440905" alias="SC_EXP_30598_2#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440905</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H3, constructed from sample accession ERS3460704 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTCGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460704">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460704</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440906" alias="SC_EXP_30598_2#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440906</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I3, constructed from sample accession ERS3460705 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460705">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460705</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656680</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440907" alias="SC_EXP_30598_2#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440907</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J3, constructed from sample accession ERS3460706 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGACGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460706">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460706</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656681</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440908" alias="SC_EXP_30598_2#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440908</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K3, constructed from sample accession ERS3460707 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTCCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460707">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460707</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656682</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440909" alias="SC_EXP_30598_2#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L3, constructed from sample accession ERS3460708 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGTGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460708">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460708</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656683</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440910" alias="SC_EXP_30598_2#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M3, constructed from sample accession ERS3460709 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TAGGCGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460709">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460709</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656684</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440911" alias="SC_EXP_30598_2#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N3, constructed from sample accession ERS3460710 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTCAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460710">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460710</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656685</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440912" alias="SC_EXP_30598_2#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O3, constructed from sample accession ERS3460711 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GACTTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460711">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460711</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656686</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440913" alias="SC_EXP_30598_2#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P3, constructed from sample accession ERS3460712 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACTCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460712">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460712</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656687</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440914" alias="SC_EXP_30598_2#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A4, constructed from sample accession ERS3460713 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGCTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460713">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460713</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656688</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440915" alias="SC_EXP_30598_2#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440915</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B4, constructed from sample accession ERS3460714 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GACTATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460714">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460714</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656689</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440916" alias="SC_EXP_30598_2#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C4, constructed from sample accession ERS3460715 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGTGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460715">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460715</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656690</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440917" alias="SC_EXP_30598_2#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D4, constructed from sample accession ERS3460716 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460716">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460716</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656691</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440918" alias="SC_EXP_30598_2#53">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E4, constructed from sample accession ERS3460717 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACAAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460717">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460717</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656692</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440919" alias="SC_EXP_30598_2#54">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F4, constructed from sample accession ERS3460718 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460718">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460718</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440920" alias="SC_EXP_30598_2#55">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G4, constructed from sample accession ERS3460719 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTAACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460719">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460719</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440921" alias="SC_EXP_30598_2#56">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H4, constructed from sample accession ERS3460720 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCGGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460720">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460720</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440922" alias="SC_EXP_30598_2#57">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I4, constructed from sample accession ERS3460721 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGCGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460721">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460721</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440923" alias="SC_EXP_30598_2#58">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J4, constructed from sample accession ERS3460722 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCCTGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460722">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460722</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440924" alias="SC_EXP_30598_2#59">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K4, constructed from sample accession ERS3460723 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCACGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460723">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460723</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440925" alias="SC_EXP_30598_2#60">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L4, constructed from sample accession ERS3460724 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCTAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460724">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460724</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440926" alias="SC_EXP_30598_2#61">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M4, constructed from sample accession ERS3460725 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAACCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460725">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460725</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440927" alias="SC_EXP_30598_2#62">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N4, constructed from sample accession ERS3460726 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTCCAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460726">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460726</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440928" alias="SC_EXP_30598_2#63">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O4, constructed from sample accession ERS3460727 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATGGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460727">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460727</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440929" alias="SC_EXP_30598_2#64">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440929</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P4, constructed from sample accession ERS3460728 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GATTAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460728">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460728</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440930" alias="SC_EXP_30598_2#65">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440930</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A5, constructed from sample accession ERS3460729 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCATCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460729">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460729</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440931" alias="SC_EXP_30598_2#66">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440931</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B5, constructed from sample accession ERS3460730 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCATGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460730">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460730</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440932" alias="SC_EXP_30598_2#67">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C5, constructed from sample accession ERS3460731 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACTTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460731">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656706</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440933" alias="SC_EXP_30598_2#68">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440933</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D5, constructed from sample accession ERS3460732 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCTTGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460732">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460732</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656707</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440934" alias="SC_EXP_30598_2#69">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E5, constructed from sample accession ERS3460733 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTAAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460733">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460733</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440935" alias="SC_EXP_30598_2#70">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F5, constructed from sample accession ERS3460734 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460734">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460734</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440936" alias="SC_EXP_30598_2#71">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440936</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G5, constructed from sample accession ERS3460735 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460735">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460735</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440937" alias="SC_EXP_30598_2#72">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440937</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H5, constructed from sample accession ERS3460736 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTTCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460736">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460736</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656711</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440938" alias="SC_EXP_30598_2#73">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I5, constructed from sample accession ERS3460737 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTCCGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460737">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460737</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656712</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440939" alias="SC_EXP_30598_2#74">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J5, constructed from sample accession ERS3460738 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTATATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460738">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460738</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656713</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440940" alias="SC_EXP_30598_2#75">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K5, constructed from sample accession ERS3460739 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCGCTAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460739">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460739</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656714</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440941" alias="SC_EXP_30598_2#76">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L5, constructed from sample accession ERS3460740 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCTAAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460740">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460740</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656715</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440942" alias="SC_EXP_30598_2#77">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M5, constructed from sample accession ERS3460741 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCCACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460741">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460741</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656716</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440943" alias="SC_EXP_30598_2#78">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N5, constructed from sample accession ERS3460742 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCGCCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460742">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460742</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656717</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440944" alias="SC_EXP_30598_2#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O5, constructed from sample accession ERS3460743 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AACTTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460743">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460743</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656718</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440945" alias="SC_EXP_30598_2#80">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P5, constructed from sample accession ERS3460744 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTGGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460744">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460744</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656719</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440946" alias="SC_EXP_30598_2#81">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A6, constructed from sample accession ERS3460745 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGATTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460745">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656720</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440947" alias="SC_EXP_30598_2#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B6, constructed from sample accession ERS3460746 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACGCCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460746">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460746</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656721</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440948" alias="SC_EXP_30598_2#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C6, constructed from sample accession ERS3460747 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AACTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460747">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460747</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656722</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440949" alias="SC_EXP_30598_2#84">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D6, constructed from sample accession ERS3460748 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCCTATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460748">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440950" alias="SC_EXP_30598_2#85">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E6, constructed from sample accession ERS3460749 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AAACGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460749">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460749</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656724</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440951" alias="SC_EXP_30598_2#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F6, constructed from sample accession ERS3460750 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460750">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460750</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656725</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440952" alias="SC_EXP_30598_2#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G6, constructed from sample accession ERS3460751 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCTCGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460751">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440953" alias="SC_EXP_30598_2#88">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H6, constructed from sample accession ERS3460752 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TACGGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460752">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460752</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656727</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440954" alias="SC_EXP_30598_2#89">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I6, constructed from sample accession ERS3460753 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTCGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460753">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460753</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656728</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440955" alias="SC_EXP_30598_2#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J6, constructed from sample accession ERS3460754 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460754">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440956" alias="SC_EXP_30598_2#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K6, constructed from sample accession ERS3460755 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCACGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460755">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460755</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656730</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440957" alias="SC_EXP_30598_2#92">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L6, constructed from sample accession ERS3460756 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGGGTTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460756">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460756</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656731</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440958" alias="SC_EXP_30598_2#93">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M6, constructed from sample accession ERS3460757 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGGCTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460757">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440959" alias="SC_EXP_30598_2#94">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N6, constructed from sample accession ERS3460758 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGATCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460758">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460758</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656733</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440960" alias="SC_EXP_30598_2#95">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O6, constructed from sample accession ERS3460759 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCTGTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460759">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460759</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656734</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440961" alias="SC_EXP_30598_2#96">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P6, constructed from sample accession ERS3460760 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCGTACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460760">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440962" alias="SC_EXP_30598_2#97">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#97</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A7, constructed from sample accession ERS3460761 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTAACTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460761">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460761</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656736</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440963" alias="SC_EXP_30598_2#98">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B7, constructed from sample accession ERS3460762 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460762">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460762</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656737</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440964" alias="SC_EXP_30598_2#99">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C7, constructed from sample accession ERS3460763 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTGCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460763">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460763</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440965" alias="SC_EXP_30598_2#100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D7, constructed from sample accession ERS3460764 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCTGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460764">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460764</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656739</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440966" alias="SC_EXP_30598_2#101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#101</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E7, constructed from sample accession ERS3460765 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTAGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460765">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656740</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440967" alias="SC_EXP_30598_2#102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F7, constructed from sample accession ERS3460766 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACGTTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460766">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460766</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440968" alias="SC_EXP_30598_2#103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G7, constructed from sample accession ERS3460767 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTGGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460767">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460767</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440969" alias="SC_EXP_30598_2#104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H7, constructed from sample accession ERS3460768 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCTTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460768">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440970" alias="SC_EXP_30598_2#105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I7, constructed from sample accession ERS3460769 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ATATGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460769">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460769</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440971" alias="SC_EXP_30598_2#106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J7, constructed from sample accession ERS3460770 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGACGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460770">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460770</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440972" alias="SC_EXP_30598_2#107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K7, constructed from sample accession ERS3460771 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460771">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440973" alias="SC_EXP_30598_2#108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L7, constructed from sample accession ERS3460772 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460772">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460772</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440974" alias="SC_EXP_30598_2#109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M7, constructed from sample accession ERS3460773 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGCCTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460773">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460773</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440975" alias="SC_EXP_30598_2#110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N7, constructed from sample accession ERS3460774 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGCATCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460774">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440976" alias="SC_EXP_30598_2#111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O7, constructed from sample accession ERS3460775 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGATAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460775">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440977" alias="SC_EXP_30598_2#112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P7, constructed from sample accession ERS3460776 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460776">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460776</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440978" alias="SC_EXP_30598_2#113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#113</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A8, constructed from sample accession ERS3460777 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460777">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440979" alias="SC_EXP_30598_2#114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B8, constructed from sample accession ERS3460778 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCATCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460778">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440980" alias="SC_EXP_30598_2#115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C8, constructed from sample accession ERS3460779 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460779">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440981" alias="SC_EXP_30598_2#116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#116</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D8, constructed from sample accession ERS3460780 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCGGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460780">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440982" alias="SC_EXP_30598_2#117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#117</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E8, constructed from sample accession ERS3460781 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAGAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460781">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440983" alias="SC_EXP_30598_2#118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440983</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#118</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F8, constructed from sample accession ERS3460782 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGCAAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460782">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440984" alias="SC_EXP_30598_2#119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#119</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G8, constructed from sample accession ERS3460783 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAAACCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460783">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440985" alias="SC_EXP_30598_2#120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#120</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H8, constructed from sample accession ERS3460784 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460784">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440986" alias="SC_EXP_30598_2#121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#121</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I8, constructed from sample accession ERS3460785 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAGACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460785">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440987" alias="SC_EXP_30598_2#122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440987</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J8, constructed from sample accession ERS3460786 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460786">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440988" alias="SC_EXP_30598_2#123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440988</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K8, constructed from sample accession ERS3460787 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460787">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440989" alias="SC_EXP_30598_2#124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440989</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L8, constructed from sample accession ERS3460788 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCGGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460788">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440990" alias="SC_EXP_30598_2#125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440990</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#125</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M8, constructed from sample accession ERS3460789 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCCGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460789">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440991" alias="SC_EXP_30598_2#126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440991</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#126</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N8, constructed from sample accession ERS3460790 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460790">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440992" alias="SC_EXP_30598_2#127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440992</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O8, constructed from sample accession ERS3460791 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460791">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460791</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440993" alias="SC_EXP_30598_2#128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440993</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P8, constructed from sample accession ERS3460792 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTAGATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460792">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460792</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440994" alias="SC_EXP_30598_2#129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#129</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A9, constructed from sample accession ERS3460793 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTCGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460793">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656768</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440995" alias="SC_EXP_30598_2#130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#130</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B9, constructed from sample accession ERS3460794 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460794">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656769</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440996" alias="SC_EXP_30598_2#131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440996</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#131</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C9, constructed from sample accession ERS3460795 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460795">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460795</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440997" alias="SC_EXP_30598_2#132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440997</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D9, constructed from sample accession ERS3460796 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460796">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440998" alias="SC_EXP_30598_2#133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440998</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#133</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E9, constructed from sample accession ERS3460797 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCATGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460797">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4440999" alias="SC_EXP_30598_2#134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4440999</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#134</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F9, constructed from sample accession ERS3460798 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTAATCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460798">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441000" alias="SC_EXP_30598_2#135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441000</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#135</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G9, constructed from sample accession ERS3460799 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGTACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460799">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441001" alias="SC_EXP_30598_2#136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441001</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H9, constructed from sample accession ERS3460800 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTATGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460800">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460800</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441002" alias="SC_EXP_30598_2#137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441002</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#137</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I9, constructed from sample accession ERS3460801 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTAAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460801">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441003" alias="SC_EXP_30598_2#138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441003</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#138</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J9, constructed from sample accession ERS3460802 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTATGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460802">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441004" alias="SC_EXP_30598_2#139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441004</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K9, constructed from sample accession ERS3460803 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460803">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460803</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441005" alias="SC_EXP_30598_2#140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441005</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L9, constructed from sample accession ERS3460804 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGTTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460804">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441006" alias="SC_EXP_30598_2#141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441006</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#141</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M9, constructed from sample accession ERS3460805 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GACGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460805">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441007" alias="SC_EXP_30598_2#142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441007</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#142</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N9, constructed from sample accession ERS3460806 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TATATTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460806">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460806</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441008" alias="SC_EXP_30598_2#143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441008</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O9, constructed from sample accession ERS3460807 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGCTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460807">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460807</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441009" alias="SC_EXP_30598_2#144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441009</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P9, constructed from sample accession ERS3460808 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGACCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460808">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441010" alias="SC_EXP_30598_2#145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441010</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#145</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A10, constructed from sample accession ERS3460813 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTCTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460813">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460813</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441011" alias="SC_EXP_30598_2#146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441011</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#146</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B10, constructed from sample accession ERS3460814 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCGGGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441012" alias="SC_EXP_30598_2#147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441012</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C10, constructed from sample accession ERS3460815 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460815">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460815</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441013" alias="SC_EXP_30598_2#148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441013</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D10, constructed from sample accession ERS3460816 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACGTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460816">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441014" alias="SC_EXP_30598_2#149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#149</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E10, constructed from sample accession ERS3460817 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAAACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460817">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656792</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441015" alias="SC_EXP_30598_2#150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441015</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#150</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F10, constructed from sample accession ERS3460818 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGTATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460818">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460818</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441016" alias="SC_EXP_30598_2#151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#151</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G10, constructed from sample accession ERS3460819 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCCATTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460819">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441017" alias="SC_EXP_30598_2#152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H10, constructed from sample accession ERS3460820 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCGTTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460820">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460820</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441018" alias="SC_EXP_30598_2#153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#153</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I10, constructed from sample accession ERS3460821 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460821">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460821</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441019" alias="SC_EXP_30598_2#154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#154</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J10, constructed from sample accession ERS3460822 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGCTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460822">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460822</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441020" alias="SC_EXP_30598_2#155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K10, constructed from sample accession ERS3460823 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCCAAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460823">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460823</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441021" alias="SC_EXP_30598_2#156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L10, constructed from sample accession ERS3460809 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTCGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460809">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460809</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441022" alias="SC_EXP_30598_2#157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441022</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#157</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M10, constructed from sample accession ERS3460810 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACTGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460810">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460810</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441023" alias="SC_EXP_30598_2#158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441023</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#158</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N10, constructed from sample accession ERS3460811 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460811">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441024" alias="SC_EXP_30598_2#159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441024</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#159</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O10, constructed from sample accession ERS3460812 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAGGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460812">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460812</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441025" alias="SC_EXP_30598_2#160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P10, constructed from sample accession ERS3460824 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AACCAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460824">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460824</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441026" alias="SC_EXP_30598_2#161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#161</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A11, constructed from sample accession ERS3460825 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460825">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441027" alias="SC_EXP_30598_2#162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#162</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B11, constructed from sample accession ERS3460826 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460826">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441028" alias="SC_EXP_30598_2#163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C11, constructed from sample accession ERS3460827 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460827">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460827</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441029" alias="SC_EXP_30598_2#164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D11, constructed from sample accession ERS3460828 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTGGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441030" alias="SC_EXP_30598_2#165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#165</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E11, constructed from sample accession ERS3460829 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GATATGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460829">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460829</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441031" alias="SC_EXP_30598_2#166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#166</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F11, constructed from sample accession ERS3460830 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCGAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460830">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441032" alias="SC_EXP_30598_2#167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#167</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G11, constructed from sample accession ERS3460831 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441033" alias="SC_EXP_30598_2#168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H11, constructed from sample accession ERS3460832 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTCGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460832">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441034" alias="SC_EXP_30598_2#169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#169</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I11, constructed from sample accession ERS3460833 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460833">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460833</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441035" alias="SC_EXP_30598_2#170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#170</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J11, constructed from sample accession ERS3460834 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ATCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460834">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441036" alias="SC_EXP_30598_2#171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K11, constructed from sample accession ERS3460835 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460835">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460835</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441037" alias="SC_EXP_30598_2#172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#172</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L11, constructed from sample accession ERS3460836 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGGGCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460836">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441038" alias="SC_EXP_30598_2#173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#173</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M11, constructed from sample accession ERS3460837 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCGGCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460837">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460837</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441039" alias="SC_EXP_30598_2#174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#174</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N11, constructed from sample accession ERS3460838 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGCACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460838">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441040" alias="SC_EXP_30598_2#175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O11, constructed from sample accession ERS3460839 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441041" alias="SC_EXP_30598_2#176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P11, constructed from sample accession ERS3460840 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAAATAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460840">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460840</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441042" alias="SC_EXP_30598_2#177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#177</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A12, constructed from sample accession ERS3460841 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460841">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441043" alias="SC_EXP_30598_2#178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441043</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#178</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B12, constructed from sample accession ERS3460842 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441044" alias="SC_EXP_30598_2#179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#179</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C12, constructed from sample accession ERS3460843 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAAAGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460843">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441045" alias="SC_EXP_30598_2#180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D12, constructed from sample accession ERS3460844 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCAAAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460844">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460844</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441046" alias="SC_EXP_30598_2#181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#181</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E12, constructed from sample accession ERS3460845 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGACGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441047" alias="SC_EXP_30598_2#182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#182</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F12, constructed from sample accession ERS3460846 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCTTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460846">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460846</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441048" alias="SC_EXP_30598_2#183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#183</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G12, constructed from sample accession ERS3460847 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGAAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460847">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460847</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441049" alias="SC_EXP_30598_2#184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#184</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H12, constructed from sample accession ERS3460848 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAGGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441050" alias="SC_EXP_30598_2#185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#185</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I12, constructed from sample accession ERS3460849 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460849">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460849</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441051" alias="SC_EXP_30598_2#186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#186</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J12, constructed from sample accession ERS3460850 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCGGGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460850">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460850</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441052" alias="SC_EXP_30598_2#187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#187</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K12, constructed from sample accession ERS3460851 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGTTGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441053" alias="SC_EXP_30598_2#188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#188</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L12, constructed from sample accession ERS3460852 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460852">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460852</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441054" alias="SC_EXP_30598_2#189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#189</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M12, constructed from sample accession ERS3460853 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCCTTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460853">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460853</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441055" alias="SC_EXP_30598_2#190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#190</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N12, constructed from sample accession ERS3460854 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCCGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441056" alias="SC_EXP_30598_2#191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#191</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O12, constructed from sample accession ERS3460855 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAGAAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460855">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460855</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441057" alias="SC_EXP_30598_2#192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#192</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P12, constructed from sample accession ERS3460856 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAAATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460856">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460856</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441058" alias="SC_EXP_30598_2#193">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#193</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#193</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A13, constructed from sample accession ERS3460857 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTACCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441059" alias="SC_EXP_30598_2#194">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#194</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B13, constructed from sample accession ERS3460858 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTTCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460858">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441060" alias="SC_EXP_30598_2#195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#195</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C13, constructed from sample accession ERS3460859 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TACGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460859">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441061" alias="SC_EXP_30598_2#196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#196</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D13, constructed from sample accession ERS3460860 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441062" alias="SC_EXP_30598_2#197">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#197</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E13, constructed from sample accession ERS3460861 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTCGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460861">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441063" alias="SC_EXP_30598_2#198">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#198</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F13, constructed from sample accession ERS3460862 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AATAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460862">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441064" alias="SC_EXP_30598_2#199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#199</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G13, constructed from sample accession ERS3460863 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCACTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441065" alias="SC_EXP_30598_2#200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#200</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H13, constructed from sample accession ERS3460864 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460864">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441066" alias="SC_EXP_30598_2#201">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#201</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I13, constructed from sample accession ERS3460865 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGATGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460865">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460865</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441067" alias="SC_EXP_30598_2#202">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#202</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#202</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J13, constructed from sample accession ERS3460866 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCGTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441068" alias="SC_EXP_30598_2#203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#203</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K13, constructed from sample accession ERS3460867 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460867">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441069" alias="SC_EXP_30598_2#204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#204</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L13, constructed from sample accession ERS3460868 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGACTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460868">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441070" alias="SC_EXP_30598_2#205">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#205</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#205</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M13, constructed from sample accession ERS3460869 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TAGTATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460869">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441071" alias="SC_EXP_30598_2#206">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#206</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N13, constructed from sample accession ERS3460870 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGGGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441072" alias="SC_EXP_30598_2#207">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#207</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O13, constructed from sample accession ERS3460871 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGACACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460871">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441073" alias="SC_EXP_30598_2#208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#208</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P13, constructed from sample accession ERS3460872 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GATATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460872">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441074" alias="SC_EXP_30598_2#209">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#209</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A14, constructed from sample accession ERS3460873 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460873">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441075" alias="SC_EXP_30598_2#210">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#210</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B14, constructed from sample accession ERS3460874 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460874">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441076" alias="SC_EXP_30598_2#211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#211</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C14, constructed from sample accession ERS3460875 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTTGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460875">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441077" alias="SC_EXP_30598_2#212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#212</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D14, constructed from sample accession ERS3460876 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460876">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441078" alias="SC_EXP_30598_2#213">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#213</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#213</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E14, constructed from sample accession ERS3460877 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGGGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460877">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441079" alias="SC_EXP_30598_2#214">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#214</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F14, constructed from sample accession ERS3460878 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCGGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460878">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441080" alias="SC_EXP_30598_2#215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#215</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G14, constructed from sample accession ERS3460879 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GACGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460879">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441081" alias="SC_EXP_30598_2#216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#216</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H14, constructed from sample accession ERS3460880 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCGGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460880">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441082" alias="SC_EXP_30598_2#217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#217</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I14, constructed from sample accession ERS3460881 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCTTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460881">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460881</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441083" alias="SC_EXP_30598_2#218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#218</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J14, constructed from sample accession ERS3460882 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460882">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460882</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441084" alias="SC_EXP_30598_2#219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#219</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K14, constructed from sample accession ERS3460883 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTTCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460883">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460883</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441085" alias="SC_EXP_30598_2#220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#220</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L14, constructed from sample accession ERS3460884 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AACGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441086" alias="SC_EXP_30598_2#221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#221</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M14, constructed from sample accession ERS3460885 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGCACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441087" alias="SC_EXP_30598_2#222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#222</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#222</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N14, constructed from sample accession ERS3460886 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441088" alias="SC_EXP_30598_2#223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#223</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O14, constructed from sample accession ERS3460887 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441089" alias="SC_EXP_30598_2#224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#224</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P14, constructed from sample accession ERS3460888 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441090" alias="SC_EXP_30598_2#225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#225</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A15, constructed from sample accession ERS3460889 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGTAGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441091" alias="SC_EXP_30598_2#226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#226</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#226</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B15, constructed from sample accession ERS3460890 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AATGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441092" alias="SC_EXP_30598_2#227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#227</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C15, constructed from sample accession ERS3460891 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441093" alias="SC_EXP_30598_2#228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#228</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D15, constructed from sample accession ERS3460892 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCAATAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441094" alias="SC_EXP_30598_2#229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#229</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E15, constructed from sample accession ERS3460893 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTGTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441095" alias="SC_EXP_30598_2#230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#230</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F15, constructed from sample accession ERS3460894 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460894">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441096" alias="SC_EXP_30598_2#231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#231</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#231</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G15, constructed from sample accession ERS3460895 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441097" alias="SC_EXP_30598_2#232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#232</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H15, constructed from sample accession ERS3460896 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460896">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460896</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441098" alias="SC_EXP_30598_2#233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#233</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I15, constructed from sample accession ERS3460897 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTGCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460897">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441099" alias="SC_EXP_30598_2#234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#234</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J15, constructed from sample accession ERS3460898 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCGCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460898">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441100" alias="SC_EXP_30598_2#235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#235</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K15, constructed from sample accession ERS3460899 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATATTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460899">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441101" alias="SC_EXP_30598_2#236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#236</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L15, constructed from sample accession ERS3460900 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCAAACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460900">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441102" alias="SC_EXP_30598_2#237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#237</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M15, constructed from sample accession ERS3460901 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCCTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460901">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441103" alias="SC_EXP_30598_2#238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#238</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N15, constructed from sample accession ERS3460902 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCGATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441104" alias="SC_EXP_30598_2#239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#239</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O15, constructed from sample accession ERS3460903 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GACTCCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460903">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441105" alias="SC_EXP_30598_2#240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#240</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P15, constructed from sample accession ERS3460904 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460904">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441106" alias="SC_EXP_30598_2#241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#241</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A16, constructed from sample accession ERS3460905 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441107" alias="SC_EXP_30598_2#242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#242</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#242</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B16, constructed from sample accession ERS3460906 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCTTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460906">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460906</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441108" alias="SC_EXP_30598_2#243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#243</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#243</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C16, constructed from sample accession ERS3460907 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTCACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460907">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460907</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441109" alias="SC_EXP_30598_2#244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#244</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#244</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D16, constructed from sample accession ERS3460908 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGGCCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441110" alias="SC_EXP_30598_2#245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#245</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E16, constructed from sample accession ERS3460909 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGGCTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460909">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460909</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441111" alias="SC_EXP_30598_2#246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#246</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F16, constructed from sample accession ERS3460910 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCTGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460910">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441112" alias="SC_EXP_30598_2#247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#247</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G16, constructed from sample accession ERS3460911 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCTCTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441113" alias="SC_EXP_30598_2#248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#248</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H16, constructed from sample accession ERS3460912 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCGGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460912">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441114" alias="SC_EXP_30598_2#249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#249</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I16, constructed from sample accession ERS3460913 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460913">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441115" alias="SC_EXP_30598_2#250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#250</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J16, constructed from sample accession ERS3460914 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441116" alias="SC_EXP_30598_2#251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#251</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K16, constructed from sample accession ERS3460915 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCGCATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460915">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441117" alias="SC_EXP_30598_2#252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#252</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L16, constructed from sample accession ERS3460916 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGACGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460916">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441118" alias="SC_EXP_30598_2#253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#253</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M16, constructed from sample accession ERS3460917 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441119" alias="SC_EXP_30598_2#254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#254</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N16, constructed from sample accession ERS3460918 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTAAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460918">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441120" alias="SC_EXP_30598_2#255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#255</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O16, constructed from sample accession ERS3460919 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTCTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460919">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441121" alias="SC_EXP_30598_2#256">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#256</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#256</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P16, constructed from sample accession ERS3460920 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTTCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460920">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441122" alias="SC_EXP_30598_2#257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#257</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A17, constructed from sample accession ERS3460921 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCACGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460921">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460921</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441123" alias="SC_EXP_30598_2#258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#258</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B17, constructed from sample accession ERS3460922 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460922">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441124" alias="SC_EXP_30598_2#259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#259</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C17, constructed from sample accession ERS3460923 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCTGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460923">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460923</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441125" alias="SC_EXP_30598_2#260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#260</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D17, constructed from sample accession ERS3460924 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCTGAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460924">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460924</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441126" alias="SC_EXP_30598_2#261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#261</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E17, constructed from sample accession ERS3460925 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCAGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441127" alias="SC_EXP_30598_2#262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#262</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#262</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F17, constructed from sample accession ERS3460926 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGAAAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460926">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460926</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441128" alias="SC_EXP_30598_2#263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#263</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#263</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G17, constructed from sample accession ERS3460927 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460927">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460927</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441129" alias="SC_EXP_30598_2#264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#264</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#264</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H17, constructed from sample accession ERS3460928 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGGTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441130" alias="SC_EXP_30598_2#265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#265</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#265</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I17, constructed from sample accession ERS3460929 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460929">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441131" alias="SC_EXP_30598_2#266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#266</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#266</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J17, constructed from sample accession ERS3460930 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460930">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460930</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441132" alias="SC_EXP_30598_2#267">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#267</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#267</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K17, constructed from sample accession ERS3460931 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TATCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441133" alias="SC_EXP_30598_2#268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#268</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#268</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L17, constructed from sample accession ERS3460932 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCAGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460932">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460932</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441134" alias="SC_EXP_30598_2#269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#269</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M17, constructed from sample accession ERS3460933 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACTGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460933">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441135" alias="SC_EXP_30598_2#270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#270</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#270</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N17, constructed from sample accession ERS3460934 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGGGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441136" alias="SC_EXP_30598_2#271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#271</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#271</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O17, constructed from sample accession ERS3460935 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGAGTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460935">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441137" alias="SC_EXP_30598_2#272">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#272</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#272</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P17, constructed from sample accession ERS3460936 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460936">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460936</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441138" alias="SC_EXP_30598_2#273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#273</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A18, constructed from sample accession ERS3460937 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGGCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460937">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441139" alias="SC_EXP_30598_2#274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#274</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#274</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B18, constructed from sample accession ERS3460938 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTGAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441140" alias="SC_EXP_30598_2#275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#275</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#275</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C18, constructed from sample accession ERS3460939 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCGCTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460939">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441141" alias="SC_EXP_30598_2#276">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#276</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#276</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D18, constructed from sample accession ERS3460940 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCCTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441142" alias="SC_EXP_30598_2#277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#277</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#277</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E18, constructed from sample accession ERS3460941 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTGCGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441143" alias="SC_EXP_30598_2#278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#278</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#278</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F18, constructed from sample accession ERS3460942 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AAAGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441144" alias="SC_EXP_30598_2#279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#279</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#279</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G18, constructed from sample accession ERS3460943 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCCGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441145" alias="SC_EXP_30598_2#280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#280</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#280</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H18, constructed from sample accession ERS3460944 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACTCGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441146" alias="SC_EXP_30598_2#281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#281</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I18, constructed from sample accession ERS3460945 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AACCGGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441147" alias="SC_EXP_30598_2#282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#282</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#282</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J18, constructed from sample accession ERS3460946 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGATTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441148" alias="SC_EXP_30598_2#283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#283</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#283</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K18, constructed from sample accession ERS3460947 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441149" alias="SC_EXP_30598_2#284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#284</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#284</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L18, constructed from sample accession ERS3460948 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTAAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441150" alias="SC_EXP_30598_2#285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#285</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M18, constructed from sample accession ERS3460949 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCTAGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441151" alias="SC_EXP_30598_2#286">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#286</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#286</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N18, constructed from sample accession ERS3460950 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCTTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441152" alias="SC_EXP_30598_2#287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#287</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#287</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O18, constructed from sample accession ERS3460951 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTATTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441153" alias="SC_EXP_30598_2#288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#288</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#288</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P18, constructed from sample accession ERS3460952 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441154" alias="SC_EXP_30598_2#289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#289</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#289</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A19, constructed from sample accession ERS3460953 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCGGAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441155" alias="SC_EXP_30598_2#290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#290</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#290</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B19, constructed from sample accession ERS3460954 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTGACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441156" alias="SC_EXP_30598_2#291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#291</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#291</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C19, constructed from sample accession ERS3460955 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTGGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460955">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441157" alias="SC_EXP_30598_2#292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#292</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#292</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D19, constructed from sample accession ERS3460956 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441158" alias="SC_EXP_30598_2#293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#293</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E19, constructed from sample accession ERS3460957 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTCAAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460957">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441159" alias="SC_EXP_30598_2#294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#294</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F19, constructed from sample accession ERS3460958 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441160" alias="SC_EXP_30598_2#295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#295</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G19, constructed from sample accession ERS3460959 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460959">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441161" alias="SC_EXP_30598_2#296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#296</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H19, constructed from sample accession ERS3460960 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441162" alias="SC_EXP_30598_2#297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#297</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I19, constructed from sample accession ERS3460961 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCTAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441163" alias="SC_EXP_30598_2#298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J19, constructed from sample accession ERS3460962 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCGTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441164" alias="SC_EXP_30598_2#299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K19, constructed from sample accession ERS3460963 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGAGGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441165" alias="SC_EXP_30598_2#300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L19, constructed from sample accession ERS3460964 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTAGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441166" alias="SC_EXP_30598_2#301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M19, constructed from sample accession ERS3460965 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGCGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441167" alias="SC_EXP_30598_2#302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N19, constructed from sample accession ERS3460966 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACGCGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441168" alias="SC_EXP_30598_2#303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#303</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O19, constructed from sample accession ERS3460967 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCGCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441169" alias="SC_EXP_30598_2#304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#304</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P19, constructed from sample accession ERS3460968 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441170" alias="SC_EXP_30598_2#305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#305</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A20, constructed from sample accession ERS3460969 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGTGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441171" alias="SC_EXP_30598_2#306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#306</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B20, constructed from sample accession ERS3460970 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441172" alias="SC_EXP_30598_2#307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#307</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C20, constructed from sample accession ERS3460971 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441173" alias="SC_EXP_30598_2#308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D20, constructed from sample accession ERS3460972 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460972">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441174" alias="SC_EXP_30598_2#309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E20, constructed from sample accession ERS3460973 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCAAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460973">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441175" alias="SC_EXP_30598_2#310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F20, constructed from sample accession ERS3460974 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence ACGTAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441176" alias="SC_EXP_30598_2#311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G20, constructed from sample accession ERS3460975 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCTATATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441177" alias="SC_EXP_30598_2#312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H20, constructed from sample accession ERS3460976 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTTCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460976">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441178" alias="SC_EXP_30598_2#313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I20, constructed from sample accession ERS3460977 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCTGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441179" alias="SC_EXP_30598_2#314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J20, constructed from sample accession ERS3460978 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGACCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460978">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441180" alias="SC_EXP_30598_2#315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#315</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K20, constructed from sample accession ERS3460979 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGTATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460979">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441181" alias="SC_EXP_30598_2#316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#316</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L20, constructed from sample accession ERS3460980 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441182" alias="SC_EXP_30598_2#317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#317</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M20, constructed from sample accession ERS3460981 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460981">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441183" alias="SC_EXP_30598_2#318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#318</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#318</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N20, constructed from sample accession ERS3460982 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGCAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460982">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441184" alias="SC_EXP_30598_2#319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O20, constructed from sample accession ERS3460983 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGGATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441185" alias="SC_EXP_30598_2#320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P20, constructed from sample accession ERS3460984 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGCGGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441186" alias="SC_EXP_30598_2#321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A21, constructed from sample accession ERS3460985 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441187" alias="SC_EXP_30598_2#322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B21, constructed from sample accession ERS3460986 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTTGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441188" alias="SC_EXP_30598_2#323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C21, constructed from sample accession ERS3460987 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCAGGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441189" alias="SC_EXP_30598_2#324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#324</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D21, constructed from sample accession ERS3460988 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441190" alias="SC_EXP_30598_2#325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#325</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E21, constructed from sample accession ERS3460989 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTGTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441191" alias="SC_EXP_30598_2#326">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#326</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#326</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F21, constructed from sample accession ERS3460990 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTTAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460990">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441192" alias="SC_EXP_30598_2#327">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#327</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#327</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G21, constructed from sample accession ERS3460991 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AAGGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441193" alias="SC_EXP_30598_2#328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#328</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#328</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H21, constructed from sample accession ERS3460992 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460992">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460992</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441194" alias="SC_EXP_30598_2#329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#329</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#329</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I21, constructed from sample accession ERS3460993 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTACTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441195" alias="SC_EXP_30598_2#330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#330</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#330</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J21, constructed from sample accession ERS3460994 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCACGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441196" alias="SC_EXP_30598_2#331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#331</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#331</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K21, constructed from sample accession ERS3460995 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCGAATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441197" alias="SC_EXP_30598_2#332">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#332</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#332</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L21, constructed from sample accession ERS3460996 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GATGAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441198" alias="SC_EXP_30598_2#333">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#333</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#333</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M21, constructed from sample accession ERS3460997 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTTTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441199" alias="SC_EXP_30598_2#334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#334</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#334</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N21, constructed from sample accession ERS3460998 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460998">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460998</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441200" alias="SC_EXP_30598_2#335">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#335</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#335</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O21, constructed from sample accession ERS3460999 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3460999">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3460999</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441201" alias="SC_EXP_30598_2#336">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#336</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#336</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P21, constructed from sample accession ERS3461000 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AACCTGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441202" alias="SC_EXP_30598_2#337">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#337</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#337</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A22, constructed from sample accession ERS3461001 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTTTCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461001">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461001</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441203" alias="SC_EXP_30598_2#338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#338</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#338</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B22, constructed from sample accession ERS3461002 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AAATGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461002">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461002</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441204" alias="SC_EXP_30598_2#339">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#339</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#339</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C22, constructed from sample accession ERS3461003 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CATCGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461003">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441205" alias="SC_EXP_30598_2#340">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#340</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#340</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D22, constructed from sample accession ERS3461004 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCACAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461004">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461004</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441206" alias="SC_EXP_30598_2#341">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#341</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#341</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E22, constructed from sample accession ERS3461005 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AGACTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461005">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441207" alias="SC_EXP_30598_2#342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#342</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#342</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F22, constructed from sample accession ERS3461006 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AATGCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441208" alias="SC_EXP_30598_2#343">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#343</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#343</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G22, constructed from sample accession ERS3461007 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GACGGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461007">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461007</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441209" alias="SC_EXP_30598_2#344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#344</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#344</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H22, constructed from sample accession ERS3461008 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGATAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441210" alias="SC_EXP_30598_2#345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#345</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#345</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I22, constructed from sample accession ERS3461009 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TAGGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461009">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441211" alias="SC_EXP_30598_2#346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#346</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#346</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J22, constructed from sample accession ERS3461010 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GAGCATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441212" alias="SC_EXP_30598_2#347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#347</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#347</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K22, constructed from sample accession ERS3461011 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441213" alias="SC_EXP_30598_2#348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#348</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#348</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L22, constructed from sample accession ERS3461012 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTCTTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461012">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441214" alias="SC_EXP_30598_2#349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#349</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#349</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M22, constructed from sample accession ERS3461013 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTAGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461013">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441215" alias="SC_EXP_30598_2#350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#350</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#350</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N22, constructed from sample accession ERS3461014 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGCCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441216" alias="SC_EXP_30598_2#351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#351</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#351</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O22, constructed from sample accession ERS3461015 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGGAGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441217" alias="SC_EXP_30598_2#352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#352</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#352</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P22, constructed from sample accession ERS3461016 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441218" alias="SC_EXP_30598_2#353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#353</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#353</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A23, constructed from sample accession ERS3461017 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTGAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461017">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441219" alias="SC_EXP_30598_2#354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#354</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#354</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B23, constructed from sample accession ERS3461018 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTTAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656994</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441220" alias="SC_EXP_30598_2#355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#355</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#355</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C23, constructed from sample accession ERS3461019 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTTGGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461019">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656995</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441221" alias="SC_EXP_30598_2#356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#356</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#356</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D23, constructed from sample accession ERS3461020 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461020">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461020</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441222" alias="SC_EXP_30598_2#357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#357</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#357</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E23, constructed from sample accession ERS3461021 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AACAGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441223" alias="SC_EXP_30598_2#358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#358</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#358</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F23, constructed from sample accession ERS3461022 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTTGTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461022">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441224" alias="SC_EXP_30598_2#359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#359</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#359</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G23, constructed from sample accession ERS3461023 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AATTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461023">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5656999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441225" alias="SC_EXP_30598_2#360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#360</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#360</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H23, constructed from sample accession ERS3461024 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence AAAGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441226" alias="SC_EXP_30598_2#361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#361</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#361</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I23, constructed from sample accession ERS3461025 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGCATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461025">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441227" alias="SC_EXP_30598_2#362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#362</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#362</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J23, constructed from sample accession ERS3461026 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TCAGTTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461026">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441228" alias="SC_EXP_30598_2#363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#363</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#363</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K23, constructed from sample accession ERS3461027 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGTTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441229" alias="SC_EXP_30598_2#364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#364</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#364</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L23, constructed from sample accession ERS3461028 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461028">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441230" alias="SC_EXP_30598_2#365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#365</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#365</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M23, constructed from sample accession ERS3461029 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGGGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441231" alias="SC_EXP_30598_2#366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#366</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#366</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N23, constructed from sample accession ERS3461030 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCAGCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441232" alias="SC_EXP_30598_2#367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#367</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#367</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O23, constructed from sample accession ERS3461031 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGTGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461031">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441233" alias="SC_EXP_30598_2#368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#368</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#368</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P23, constructed from sample accession ERS3461032 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGCCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441234" alias="SC_EXP_30598_2#369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#369</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#369</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:A24, constructed from sample accession ERS3461033 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGCACCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441235" alias="SC_EXP_30598_2#370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#370</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#370</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:B24, constructed from sample accession ERS3461034 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CCGATCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461034">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:B24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441236" alias="SC_EXP_30598_2#371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#371</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#371</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:C24, constructed from sample accession ERS3461035 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CAAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461035">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441237" alias="SC_EXP_30598_2#372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#372</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#372</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:D24, constructed from sample accession ERS3461036 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GGCGTCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657012</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:D24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441238" alias="SC_EXP_30598_2#373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#373</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#373</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:E24, constructed from sample accession ERS3461037 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTAGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461037">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441239" alias="SC_EXP_30598_2#374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#374</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#374</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:F24, constructed from sample accession ERS3461038 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GTCGGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461038">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657014</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:F24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441240" alias="SC_EXP_30598_2#375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#375</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#375</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:G24, constructed from sample accession ERS3461039 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCCTCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657015</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441241" alias="SC_EXP_30598_2#376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#376</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#376</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:H24, constructed from sample accession ERS3461040 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTATACCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461040">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:H24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441242" alias="SC_EXP_30598_2#377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#377</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#377</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:I24, constructed from sample accession ERS3461041 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TGGTCGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461041">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657017</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441243" alias="SC_EXP_30598_2#378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#378</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#378</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:J24, constructed from sample accession ERS3461042 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTAAACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:J24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441244" alias="SC_EXP_30598_2#379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#379</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#379</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:K24, constructed from sample accession ERS3461043 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CGTTGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441245" alias="SC_EXP_30598_2#380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#380</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#380</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:L24, constructed from sample accession ERS3461044 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CACTCTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461044">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:L24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441246" alias="SC_EXP_30598_2#381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#381</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#381</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:M24, constructed from sample accession ERS3461045 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TTGTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461045">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657021</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441247" alias="SC_EXP_30598_2#382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#382</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#382</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:N24, constructed from sample accession ERS3461046 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence GCAGCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:N24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441248" alias="SC_EXP_30598_2#383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#383</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#383</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:O24, constructed from sample accession ERS3461047 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence CTGCCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441249" alias="SC_EXP_30598_2#384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_2#384</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_2#384</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571073W:P24, constructed from sample accession ERS3461048 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_2).  This submission includes reads tagged with the sequence TACCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461048">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571073W:P24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441250" alias="SC_EXP_30598_3#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A1, constructed from sample accession ERS3461049 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441251" alias="SC_EXP_30598_3#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B1, constructed from sample accession ERS3461050 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCGTTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461050">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441252" alias="SC_EXP_30598_3#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C1, constructed from sample accession ERS3461051 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTAACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461051">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441253" alias="SC_EXP_30598_3#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D1, constructed from sample accession ERS3461052 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCGACTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441254" alias="SC_EXP_30598_3#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E1, constructed from sample accession ERS3461053 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATTTATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441255" alias="SC_EXP_30598_3#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F1, constructed from sample accession ERS3461054 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTAAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461054">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441256" alias="SC_EXP_30598_3#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G1, constructed from sample accession ERS3461055 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTAGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441257" alias="SC_EXP_30598_3#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H1, constructed from sample accession ERS3461056 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441258" alias="SC_EXP_30598_3#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I1, constructed from sample accession ERS3461057 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTGATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441259" alias="SC_EXP_30598_3#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J1, constructed from sample accession ERS3461058 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCTCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461058">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441260" alias="SC_EXP_30598_3#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K1, constructed from sample accession ERS3461059 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TATTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461059">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461059</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441261" alias="SC_EXP_30598_3#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L1, constructed from sample accession ERS3461060 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCTCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461060">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461060</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441262" alias="SC_EXP_30598_3#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M1, constructed from sample accession ERS3461061 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTACGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461061">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461061</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441263" alias="SC_EXP_30598_3#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N1, constructed from sample accession ERS3461062 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCGGGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461062">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461062</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441264" alias="SC_EXP_30598_3#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O1, constructed from sample accession ERS3461063 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461063">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461063</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441265" alias="SC_EXP_30598_3#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P1, constructed from sample accession ERS3461064 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461064">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461064</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441266" alias="SC_EXP_30598_3#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A2, constructed from sample accession ERS3461066 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461066">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461066</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441267" alias="SC_EXP_30598_3#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B2, constructed from sample accession ERS3461067 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461067">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461067</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441268" alias="SC_EXP_30598_3#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C2, constructed from sample accession ERS3461068 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GATACTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461068">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461068</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441269" alias="SC_EXP_30598_3#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D2, constructed from sample accession ERS3461069 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461069">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441270" alias="SC_EXP_30598_3#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E2, constructed from sample accession ERS3461070 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCAAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461070">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461070</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441271" alias="SC_EXP_30598_3#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F2, constructed from sample accession ERS3461071 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTCGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461071">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461071</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441272" alias="SC_EXP_30598_3#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G2, constructed from sample accession ERS3461072 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCGGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461072">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461072</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441273" alias="SC_EXP_30598_3#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H2, constructed from sample accession ERS3461073 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTCATATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461073">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461073</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441274" alias="SC_EXP_30598_3#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I2, constructed from sample accession ERS3461074 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCTTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461074">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461074</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441275" alias="SC_EXP_30598_3#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J2, constructed from sample accession ERS3461075 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461075">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461075</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441276" alias="SC_EXP_30598_3#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K2, constructed from sample accession ERS3461076 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCACTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461076">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461076</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441277" alias="SC_EXP_30598_3#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L2, constructed from sample accession ERS3461065 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCGATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461065">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461065</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441278" alias="SC_EXP_30598_3#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M2, constructed from sample accession ERS3461077 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461077">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461077</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441279" alias="SC_EXP_30598_3#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N2, constructed from sample accession ERS3461078 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461078">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461078</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441280" alias="SC_EXP_30598_3#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O2, constructed from sample accession ERS3461079 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461079">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461079</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441281" alias="SC_EXP_30598_3#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P2, constructed from sample accession ERS3461080 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461080">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461080</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441282" alias="SC_EXP_30598_3#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A3, constructed from sample accession ERS3461081 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TATATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461081">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461081</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441283" alias="SC_EXP_30598_3#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B3, constructed from sample accession ERS3461082 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461082">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441284" alias="SC_EXP_30598_3#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C3, constructed from sample accession ERS3461083 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTATCCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461083">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441285" alias="SC_EXP_30598_3#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D3, constructed from sample accession ERS3461084 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCCACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441286" alias="SC_EXP_30598_3#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E3, constructed from sample accession ERS3461085 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTACCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441287" alias="SC_EXP_30598_3#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F3, constructed from sample accession ERS3461086 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCCTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441288" alias="SC_EXP_30598_3#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G3, constructed from sample accession ERS3461087 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAGAGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441289" alias="SC_EXP_30598_3#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H3, constructed from sample accession ERS3461088 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTCGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461088">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441290" alias="SC_EXP_30598_3#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I3, constructed from sample accession ERS3461089 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461089">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441291" alias="SC_EXP_30598_3#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J3, constructed from sample accession ERS3461090 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGACGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461090">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441292" alias="SC_EXP_30598_3#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K3, constructed from sample accession ERS3461091 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTCCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461091">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441293" alias="SC_EXP_30598_3#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L3, constructed from sample accession ERS3461092 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGTGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461092">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441294" alias="SC_EXP_30598_3#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M3, constructed from sample accession ERS3461093 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TAGGCGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461093">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441295" alias="SC_EXP_30598_3#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N3, constructed from sample accession ERS3461094 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTCAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461094">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441296" alias="SC_EXP_30598_3#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O3, constructed from sample accession ERS3461095 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GACTTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461095">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441297" alias="SC_EXP_30598_3#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P3, constructed from sample accession ERS3461096 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACTCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461096">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441298" alias="SC_EXP_30598_3#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A4, constructed from sample accession ERS3461097 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGCTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657073</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441299" alias="SC_EXP_30598_3#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B4, constructed from sample accession ERS3461098 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GACTATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441300" alias="SC_EXP_30598_3#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C4, constructed from sample accession ERS3461099 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGTGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461099">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657075</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441301" alias="SC_EXP_30598_3#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D4, constructed from sample accession ERS3461100 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461100">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657076</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441302" alias="SC_EXP_30598_3#53">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E4, constructed from sample accession ERS3461101 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACAAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461101">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461101</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657077</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441303" alias="SC_EXP_30598_3#54">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F4, constructed from sample accession ERS3461102 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461102">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657078</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441304" alias="SC_EXP_30598_3#55">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G4, constructed from sample accession ERS3461103 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTAACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461103">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657079</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441305" alias="SC_EXP_30598_3#56">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H4, constructed from sample accession ERS3461104 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCGGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461104">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461104</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441306" alias="SC_EXP_30598_3#57">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I4, constructed from sample accession ERS3461105 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGCGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657081</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441307" alias="SC_EXP_30598_3#58">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J4, constructed from sample accession ERS3461106 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCCTGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441308" alias="SC_EXP_30598_3#59">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K4, constructed from sample accession ERS3461107 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCACGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461107">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657083</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441309" alias="SC_EXP_30598_3#60">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L4, constructed from sample accession ERS3461108 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCTAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441310" alias="SC_EXP_30598_3#61">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M4, constructed from sample accession ERS3461109 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAACCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441311" alias="SC_EXP_30598_3#62">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N4, constructed from sample accession ERS3461110 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTCCAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657086</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441312" alias="SC_EXP_30598_3#63">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O4, constructed from sample accession ERS3461111 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATGGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441313" alias="SC_EXP_30598_3#64">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P4, constructed from sample accession ERS3461112 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GATTAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441314" alias="SC_EXP_30598_3#65">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A5, constructed from sample accession ERS3461113 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCATCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441315" alias="SC_EXP_30598_3#66">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B5, constructed from sample accession ERS3461114 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCATGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657090</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441316" alias="SC_EXP_30598_3#67">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C5, constructed from sample accession ERS3461115 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACTTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441317" alias="SC_EXP_30598_3#68">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D5, constructed from sample accession ERS3461116 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCTTGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441318" alias="SC_EXP_30598_3#69">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E5, constructed from sample accession ERS3461117 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTAAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441319" alias="SC_EXP_30598_3#70">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F5, constructed from sample accession ERS3461118 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441320" alias="SC_EXP_30598_3#71">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G5, constructed from sample accession ERS3461119 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441321" alias="SC_EXP_30598_3#72">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H5, constructed from sample accession ERS3461120 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTTCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441322" alias="SC_EXP_30598_3#73">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I5, constructed from sample accession ERS3461121 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTCCGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441323" alias="SC_EXP_30598_3#74">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J5, constructed from sample accession ERS3461122 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTATATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441324" alias="SC_EXP_30598_3#75">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K5, constructed from sample accession ERS3461123 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCGCTAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441325" alias="SC_EXP_30598_3#76">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L5, constructed from sample accession ERS3461124 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCTAAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441326" alias="SC_EXP_30598_3#77">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M5, constructed from sample accession ERS3461125 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCCACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441327" alias="SC_EXP_30598_3#78">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N5, constructed from sample accession ERS3461126 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCGCCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441328" alias="SC_EXP_30598_3#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O5, constructed from sample accession ERS3461127 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AACTTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441329" alias="SC_EXP_30598_3#80">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P5, constructed from sample accession ERS3461128 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTGGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441330" alias="SC_EXP_30598_3#81">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A6, constructed from sample accession ERS3461129 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGATTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441331" alias="SC_EXP_30598_3#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B6, constructed from sample accession ERS3461130 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACGCCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441332" alias="SC_EXP_30598_3#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C6, constructed from sample accession ERS3461131 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AACTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441333" alias="SC_EXP_30598_3#84">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D6, constructed from sample accession ERS3461132 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCCTATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441334" alias="SC_EXP_30598_3#85">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E6, constructed from sample accession ERS3461133 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AAACGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461133">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441335" alias="SC_EXP_30598_3#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F6, constructed from sample accession ERS3461134 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441336" alias="SC_EXP_30598_3#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G6, constructed from sample accession ERS3461135 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCTCGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441337" alias="SC_EXP_30598_3#88">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H6, constructed from sample accession ERS3461136 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TACGGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441338" alias="SC_EXP_30598_3#89">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I6, constructed from sample accession ERS3461137 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTCGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441339" alias="SC_EXP_30598_3#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J6, constructed from sample accession ERS3461138 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461138">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441340" alias="SC_EXP_30598_3#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K6, constructed from sample accession ERS3461139 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCACGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461139">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441341" alias="SC_EXP_30598_3#92">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L6, constructed from sample accession ERS3461140 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGGGTTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461140">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441342" alias="SC_EXP_30598_3#93">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M6, constructed from sample accession ERS3461141 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGGCTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461141">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441343" alias="SC_EXP_30598_3#94">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N6, constructed from sample accession ERS3461142 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGATCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461142">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441344" alias="SC_EXP_30598_3#95">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O6, constructed from sample accession ERS3461143 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCTGTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461143">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441345" alias="SC_EXP_30598_3#96">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P6, constructed from sample accession ERS3461144 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCGTACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461144">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441346" alias="SC_EXP_30598_3#97">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#97</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A7, constructed from sample accession ERS3461145 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTAACTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461145">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441347" alias="SC_EXP_30598_3#98">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B7, constructed from sample accession ERS3461146 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461146">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441348" alias="SC_EXP_30598_3#99">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C7, constructed from sample accession ERS3461147 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTGCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441349" alias="SC_EXP_30598_3#100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D7, constructed from sample accession ERS3461148 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCTGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461148">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441350" alias="SC_EXP_30598_3#101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#101</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E7, constructed from sample accession ERS3461149 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTAGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461149">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441351" alias="SC_EXP_30598_3#102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F7, constructed from sample accession ERS3461150 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACGTTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441352" alias="SC_EXP_30598_3#103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G7, constructed from sample accession ERS3461151 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTGGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461151">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441353" alias="SC_EXP_30598_3#104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H7, constructed from sample accession ERS3461152 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCTTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461152">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441354" alias="SC_EXP_30598_3#105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I7, constructed from sample accession ERS3461153 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ATATGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461153">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441355" alias="SC_EXP_30598_3#106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J7, constructed from sample accession ERS3461154 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGACGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461154">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441356" alias="SC_EXP_30598_3#107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K7, constructed from sample accession ERS3461155 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461155">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441357" alias="SC_EXP_30598_3#108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L7, constructed from sample accession ERS3461156 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461156">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441358" alias="SC_EXP_30598_3#109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M7, constructed from sample accession ERS3461157 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGCCTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461157">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441359" alias="SC_EXP_30598_3#110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N7, constructed from sample accession ERS3461158 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGCATCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461158">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441360" alias="SC_EXP_30598_3#111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O7, constructed from sample accession ERS3461159 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGATAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461159">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441361" alias="SC_EXP_30598_3#112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P7, constructed from sample accession ERS3461160 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461160">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461160</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441362" alias="SC_EXP_30598_3#113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#113</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A8, constructed from sample accession ERS3461161 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461161">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441363" alias="SC_EXP_30598_3#114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B8, constructed from sample accession ERS3461162 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCATCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461162">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461162</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441364" alias="SC_EXP_30598_3#115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C8, constructed from sample accession ERS3461163 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461163">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441365" alias="SC_EXP_30598_3#116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#116</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D8, constructed from sample accession ERS3461164 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCGGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441366" alias="SC_EXP_30598_3#117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#117</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E8, constructed from sample accession ERS3461165 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAGAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461165">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461165</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441367" alias="SC_EXP_30598_3#118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#118</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F8, constructed from sample accession ERS3461166 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGCAAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461166">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461166</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441368" alias="SC_EXP_30598_3#119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#119</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G8, constructed from sample accession ERS3461167 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAAACCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461167">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441369" alias="SC_EXP_30598_3#120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#120</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H8, constructed from sample accession ERS3461168 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461168">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441370" alias="SC_EXP_30598_3#121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#121</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I8, constructed from sample accession ERS3461169 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAGACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461169">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461169</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441371" alias="SC_EXP_30598_3#122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J8, constructed from sample accession ERS3461170 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461170">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441372" alias="SC_EXP_30598_3#123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K8, constructed from sample accession ERS3461171 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461171">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461171</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441373" alias="SC_EXP_30598_3#124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L8, constructed from sample accession ERS3461172 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCGGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461172">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441374" alias="SC_EXP_30598_3#125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#125</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M8, constructed from sample accession ERS3461173 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCCGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461173">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441375" alias="SC_EXP_30598_3#126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#126</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N8, constructed from sample accession ERS3461174 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461174">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441376" alias="SC_EXP_30598_3#127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O8, constructed from sample accession ERS3461175 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461175">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441377" alias="SC_EXP_30598_3#128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P8, constructed from sample accession ERS3461176 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTAGATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461176">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441378" alias="SC_EXP_30598_3#129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#129</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A9, constructed from sample accession ERS3461177 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTCGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461177">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441379" alias="SC_EXP_30598_3#130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#130</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B9, constructed from sample accession ERS3461178 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461178">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441380" alias="SC_EXP_30598_3#131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#131</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C9, constructed from sample accession ERS3461179 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461179">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441381" alias="SC_EXP_30598_3#132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D9, constructed from sample accession ERS3461180 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461180">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461180</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441382" alias="SC_EXP_30598_3#133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#133</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E9, constructed from sample accession ERS3461181 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCATGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461181">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461181</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441383" alias="SC_EXP_30598_3#134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#134</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F9, constructed from sample accession ERS3461182 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTAATCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461182">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461182</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441384" alias="SC_EXP_30598_3#135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#135</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G9, constructed from sample accession ERS3461183 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGTACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461183">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461183</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441385" alias="SC_EXP_30598_3#136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H9, constructed from sample accession ERS3461184 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTATGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461184">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441386" alias="SC_EXP_30598_3#137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#137</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I9, constructed from sample accession ERS3461185 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTAAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461185">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441387" alias="SC_EXP_30598_3#138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#138</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J9, constructed from sample accession ERS3461186 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTATGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461186">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441388" alias="SC_EXP_30598_3#139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K9, constructed from sample accession ERS3461187 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461187">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441389" alias="SC_EXP_30598_3#140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L9, constructed from sample accession ERS3461188 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGTTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461188">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441390" alias="SC_EXP_30598_3#141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#141</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M9, constructed from sample accession ERS3461189 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GACGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461189">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461189</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441391" alias="SC_EXP_30598_3#142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#142</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N9, constructed from sample accession ERS3461190 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TATATTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461190">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461190</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441392" alias="SC_EXP_30598_3#143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O9, constructed from sample accession ERS3461191 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGCTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461191">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441393" alias="SC_EXP_30598_3#144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P9, constructed from sample accession ERS3461192 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGACCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461192">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461192</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441394" alias="SC_EXP_30598_3#145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#145</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A10, constructed from sample accession ERS3461193 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTCTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461193">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461193</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441395" alias="SC_EXP_30598_3#146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#146</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B10, constructed from sample accession ERS3461194 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCGGGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461194">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461194</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441396" alias="SC_EXP_30598_3#147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C10, constructed from sample accession ERS3461195 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461195">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441397" alias="SC_EXP_30598_3#148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D10, constructed from sample accession ERS3461196 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACGTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461196">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461196</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441398" alias="SC_EXP_30598_3#149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#149</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E10, constructed from sample accession ERS3461197 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAAACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461197">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461197</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441399" alias="SC_EXP_30598_3#150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#150</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F10, constructed from sample accession ERS3461198 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGTATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461198">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461198</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441400" alias="SC_EXP_30598_3#151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#151</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G10, constructed from sample accession ERS3461199 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCCATTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461199">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461199</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441401" alias="SC_EXP_30598_3#152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H10, constructed from sample accession ERS3461200 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCGTTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461200">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461200</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441402" alias="SC_EXP_30598_3#153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#153</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I10, constructed from sample accession ERS3461201 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461201">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461201</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441403" alias="SC_EXP_30598_3#154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#154</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J10, constructed from sample accession ERS3461202 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGCTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461202">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461202</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441404" alias="SC_EXP_30598_3#155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K10, constructed from sample accession ERS3461203 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCCAAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461203">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461203</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441405" alias="SC_EXP_30598_3#156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L10, constructed from sample accession ERS3461204 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTCGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461204">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461204</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441406" alias="SC_EXP_30598_3#157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#157</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M10, constructed from sample accession ERS3461205 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACTGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461205">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461205</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441407" alias="SC_EXP_30598_3#158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#158</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N10, constructed from sample accession ERS3461206 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461206">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461206</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441408" alias="SC_EXP_30598_3#159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#159</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O10, constructed from sample accession ERS3461207 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAGGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461207">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461207</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441409" alias="SC_EXP_30598_3#160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P10, constructed from sample accession ERS3461208 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AACCAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461208">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461208</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441410" alias="SC_EXP_30598_3#161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#161</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A11, constructed from sample accession ERS3461209 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461209">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461209</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441411" alias="SC_EXP_30598_3#162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#162</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B11, constructed from sample accession ERS3461210 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461210">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461210</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441412" alias="SC_EXP_30598_3#163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C11, constructed from sample accession ERS3461211 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441413" alias="SC_EXP_30598_3#164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D11, constructed from sample accession ERS3461212 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTGGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441414" alias="SC_EXP_30598_3#165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#165</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E11, constructed from sample accession ERS3461213 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GATATGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461213">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461213</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441415" alias="SC_EXP_30598_3#166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#166</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F11, constructed from sample accession ERS3461214 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCGAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461214">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461214</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441417" alias="SC_EXP_30598_3#168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H11, constructed from sample accession ERS3461216 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTCGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461216">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461216</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441418" alias="SC_EXP_30598_3#169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#169</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I11, constructed from sample accession ERS3461217 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461217">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461217</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657193</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441419" alias="SC_EXP_30598_3#170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#170</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J11, constructed from sample accession ERS3461218 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ATCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441420" alias="SC_EXP_30598_3#171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K11, constructed from sample accession ERS3461219 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441421" alias="SC_EXP_30598_3#172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#172</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L11, constructed from sample accession ERS3461220 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGGGCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657196</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441422" alias="SC_EXP_30598_3#173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#173</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M11, constructed from sample accession ERS3461221 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCGGCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441423" alias="SC_EXP_30598_3#174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#174</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N11, constructed from sample accession ERS3461222 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGCACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461222">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461222</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441424" alias="SC_EXP_30598_3#175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O11, constructed from sample accession ERS3461223 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461223">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657199</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441425" alias="SC_EXP_30598_3#176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P11, constructed from sample accession ERS3461224 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAAATAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461224">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461224</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441426" alias="SC_EXP_30598_3#177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#177</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A12, constructed from sample accession ERS3461225 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441427" alias="SC_EXP_30598_3#178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#178</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B12, constructed from sample accession ERS3461226 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441428" alias="SC_EXP_30598_3#179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#179</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C12, constructed from sample accession ERS3461227 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAAAGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461227">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461227</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441429" alias="SC_EXP_30598_3#180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D12, constructed from sample accession ERS3461228 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCAAAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441430" alias="SC_EXP_30598_3#181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#181</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E12, constructed from sample accession ERS3461229 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGACGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441431" alias="SC_EXP_30598_3#182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#182</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F12, constructed from sample accession ERS3461230 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCTTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461230">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461230</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441432" alias="SC_EXP_30598_3#183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#183</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G12, constructed from sample accession ERS3461231 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGAAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441433" alias="SC_EXP_30598_3#184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#184</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H12, constructed from sample accession ERS3461232 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAGGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441434" alias="SC_EXP_30598_3#185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#185</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I12, constructed from sample accession ERS3461233 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441435" alias="SC_EXP_30598_3#186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#186</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J12, constructed from sample accession ERS3461234 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCGGGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461234">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441436" alias="SC_EXP_30598_3#187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#187</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K12, constructed from sample accession ERS3461235 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGTTGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441437" alias="SC_EXP_30598_3#188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#188</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L12, constructed from sample accession ERS3461236 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657212</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441438" alias="SC_EXP_30598_3#189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#189</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M12, constructed from sample accession ERS3461237 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCCTTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461237">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441439" alias="SC_EXP_30598_3#190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#190</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N12, constructed from sample accession ERS3461238 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCCGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461238">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657214</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441440" alias="SC_EXP_30598_3#191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#191</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O12, constructed from sample accession ERS3461239 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAGAAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461239">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441441" alias="SC_EXP_30598_3#192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#192</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P12, constructed from sample accession ERS3461240 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAAATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441442" alias="SC_EXP_30598_3#193">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#193</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#193</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A13, constructed from sample accession ERS3461241 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTACCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441444" alias="SC_EXP_30598_3#195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#195</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C13, constructed from sample accession ERS3461243 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TACGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441445" alias="SC_EXP_30598_3#196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#196</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D13, constructed from sample accession ERS3461244 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657220</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441447" alias="SC_EXP_30598_3#198">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#198</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F13, constructed from sample accession ERS3461246 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AATAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461246">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461246</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657222</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441448" alias="SC_EXP_30598_3#199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#199</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G13, constructed from sample accession ERS3461247 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCACTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441450" alias="SC_EXP_30598_3#201">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#201</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I13, constructed from sample accession ERS3461249 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGATGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461249">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441451" alias="SC_EXP_30598_3#202">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#202</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#202</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J13, constructed from sample accession ERS3461250 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCGTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461250">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657226</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441453" alias="SC_EXP_30598_3#204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#204</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L13, constructed from sample accession ERS3461252 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGACTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441454" alias="SC_EXP_30598_3#205">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#205</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#205</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M13, constructed from sample accession ERS3461253 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TAGTATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461253">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657229</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441456" alias="SC_EXP_30598_3#207">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#207</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O13, constructed from sample accession ERS3461255 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGACACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441457" alias="SC_EXP_30598_3#208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#208</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P13, constructed from sample accession ERS3461256 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GATATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461256">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461256</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441459" alias="SC_EXP_30598_3#210">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#210</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B14, constructed from sample accession ERS3461258 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441460" alias="SC_EXP_30598_3#211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#211</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C14, constructed from sample accession ERS3461259 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTTGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461259">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441462" alias="SC_EXP_30598_3#213">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441462</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#213</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#213</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E14, constructed from sample accession ERS3461261 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGGGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657237</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441463" alias="SC_EXP_30598_3#214">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#214</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F14, constructed from sample accession ERS3461262 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCGGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461262">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461262</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441465" alias="SC_EXP_30598_3#216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441465</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#216</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H14, constructed from sample accession ERS3461264 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCGGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657240</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441466" alias="SC_EXP_30598_3#217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#217</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I14, constructed from sample accession ERS3461265 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCTTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461265">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461265</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441468" alias="SC_EXP_30598_3#219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#219</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K14, constructed from sample accession ERS3461267 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTTCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461267">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461267</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657243</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441469" alias="SC_EXP_30598_3#220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#220</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L14, constructed from sample accession ERS3461268 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AACGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461268">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461268</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657244</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441471" alias="SC_EXP_30598_3#222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#222</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#222</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N14, constructed from sample accession ERS3461270 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657246</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441472" alias="SC_EXP_30598_3#223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#223</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O14, constructed from sample accession ERS3461271 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461271">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657247</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441474" alias="SC_EXP_30598_3#225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#225</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A15, constructed from sample accession ERS3461273 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGTAGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657249</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441475" alias="SC_EXP_30598_3#226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#226</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#226</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B15, constructed from sample accession ERS3461274 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AATGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657250</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441477" alias="SC_EXP_30598_3#228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#228</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D15, constructed from sample accession ERS3461276 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCAATAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657252</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441478" alias="SC_EXP_30598_3#229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#229</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E15, constructed from sample accession ERS3461277 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTGTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657253</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441480" alias="SC_EXP_30598_3#231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#231</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#231</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G15, constructed from sample accession ERS3461279 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657255</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441481" alias="SC_EXP_30598_3#232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#232</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H15, constructed from sample accession ERS3461280 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657256</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441483" alias="SC_EXP_30598_3#234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#234</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J15, constructed from sample accession ERS3461282 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCGCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441484" alias="SC_EXP_30598_3#235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#235</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K15, constructed from sample accession ERS3461283 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATATTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461283">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441486" alias="SC_EXP_30598_3#237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#237</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M15, constructed from sample accession ERS3461285 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCCTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461285">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441487" alias="SC_EXP_30598_3#238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#238</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N15, constructed from sample accession ERS3461286 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCGATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461286">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461286</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441489" alias="SC_EXP_30598_3#240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#240</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P15, constructed from sample accession ERS3461288 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461288">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441490" alias="SC_EXP_30598_3#241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#241</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A16, constructed from sample accession ERS3461289 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441492" alias="SC_EXP_30598_3#243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#243</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#243</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C16, constructed from sample accession ERS3461291 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTCACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461291">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657267</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441493" alias="SC_EXP_30598_3#244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#244</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#244</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D16, constructed from sample accession ERS3461292 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGGCCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441495" alias="SC_EXP_30598_3#246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#246</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F16, constructed from sample accession ERS3461294 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCTGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441496" alias="SC_EXP_30598_3#247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#247</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G16, constructed from sample accession ERS3461295 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCTCTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441498" alias="SC_EXP_30598_3#249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#249</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I16, constructed from sample accession ERS3461297 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461297">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441499" alias="SC_EXP_30598_3#250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#250</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J16, constructed from sample accession ERS3461298 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441501" alias="SC_EXP_30598_3#252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#252</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L16, constructed from sample accession ERS3461300 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGACGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441502" alias="SC_EXP_30598_3#253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#253</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M16, constructed from sample accession ERS3461301 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657277</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441504" alias="SC_EXP_30598_3#255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#255</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O16, constructed from sample accession ERS3461303 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTCTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657279</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441505" alias="SC_EXP_30598_3#256">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#256</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#256</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P16, constructed from sample accession ERS3461304 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTTCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657280</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441507" alias="SC_EXP_30598_3#258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#258</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B17, constructed from sample accession ERS3461306 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441508" alias="SC_EXP_30598_3#259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#259</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C17, constructed from sample accession ERS3461307 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCTGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441510" alias="SC_EXP_30598_3#261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#261</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E17, constructed from sample accession ERS3461309 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCAGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441511" alias="SC_EXP_30598_3#262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#262</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#262</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F17, constructed from sample accession ERS3461310 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGAAAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441416" alias="SC_EXP_30598_3#167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#167</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G11, constructed from sample accession ERS3461215 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461215">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461215</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441443" alias="SC_EXP_30598_3#194">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#194</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B13, constructed from sample accession ERS3461242 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTTCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461242">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441446" alias="SC_EXP_30598_3#197">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#197</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E13, constructed from sample accession ERS3461245 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTCGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657221</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441449" alias="SC_EXP_30598_3#200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#200</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H13, constructed from sample accession ERS3461248 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461248">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441452" alias="SC_EXP_30598_3#203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#203</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K13, constructed from sample accession ERS3461251 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441455" alias="SC_EXP_30598_3#206">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#206</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N13, constructed from sample accession ERS3461254 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGGGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441458" alias="SC_EXP_30598_3#209">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#209</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A14, constructed from sample accession ERS3461257 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441461" alias="SC_EXP_30598_3#212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#212</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D14, constructed from sample accession ERS3461260 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461260">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461260</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657236</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441464" alias="SC_EXP_30598_3#215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441464</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#215</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G14, constructed from sample accession ERS3461263 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GACGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441467" alias="SC_EXP_30598_3#218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#218</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J14, constructed from sample accession ERS3461266 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657242</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441470" alias="SC_EXP_30598_3#221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#221</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M14, constructed from sample accession ERS3461269 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGCACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441473" alias="SC_EXP_30598_3#224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#224</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P14, constructed from sample accession ERS3461272 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441476" alias="SC_EXP_30598_3#227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#227</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C15, constructed from sample accession ERS3461275 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441479" alias="SC_EXP_30598_3#230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#230</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F15, constructed from sample accession ERS3461278 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441482" alias="SC_EXP_30598_3#233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#233</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I15, constructed from sample accession ERS3461281 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTGCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441485" alias="SC_EXP_30598_3#236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#236</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L15, constructed from sample accession ERS3461284 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCAAACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441488" alias="SC_EXP_30598_3#239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#239</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O15, constructed from sample accession ERS3461287 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GACTCCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461287">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461287</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441491" alias="SC_EXP_30598_3#242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#242</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#242</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B16, constructed from sample accession ERS3461290 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCTTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441494" alias="SC_EXP_30598_3#245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#245</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E16, constructed from sample accession ERS3461293 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGGCTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441497" alias="SC_EXP_30598_3#248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#248</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H16, constructed from sample accession ERS3461296 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCGGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657272</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441500" alias="SC_EXP_30598_3#251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#251</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K16, constructed from sample accession ERS3461299 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCGCATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657275</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441503" alias="SC_EXP_30598_3#254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#254</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N16, constructed from sample accession ERS3461302 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTAAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441506" alias="SC_EXP_30598_3#257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#257</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A17, constructed from sample accession ERS3461305 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCACGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441509" alias="SC_EXP_30598_3#260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#260</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D17, constructed from sample accession ERS3461308 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCTGAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657284</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441512" alias="SC_EXP_30598_3#263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#263</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#263</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G17, constructed from sample accession ERS3461311 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441513" alias="SC_EXP_30598_3#264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#264</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#264</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H17, constructed from sample accession ERS3461312 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGGTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657288</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441514" alias="SC_EXP_30598_3#265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#265</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#265</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I17, constructed from sample accession ERS3461313 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657289</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441515" alias="SC_EXP_30598_3#266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#266</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#266</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J17, constructed from sample accession ERS3461314 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657290</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441516" alias="SC_EXP_30598_3#267">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#267</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#267</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K17, constructed from sample accession ERS3461315 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TATCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441517" alias="SC_EXP_30598_3#268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#268</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#268</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L17, constructed from sample accession ERS3461316 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCAGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657292</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441518" alias="SC_EXP_30598_3#269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#269</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M17, constructed from sample accession ERS3461317 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACTGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461317">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657293</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441519" alias="SC_EXP_30598_3#270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#270</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#270</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N17, constructed from sample accession ERS3461318 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGGGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441520" alias="SC_EXP_30598_3#271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#271</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#271</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O17, constructed from sample accession ERS3461319 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGAGTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657295</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441521" alias="SC_EXP_30598_3#272">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#272</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#272</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P17, constructed from sample accession ERS3461320 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657296</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441522" alias="SC_EXP_30598_3#273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#273</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A18, constructed from sample accession ERS3461321 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGGCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441523" alias="SC_EXP_30598_3#274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#274</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#274</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B18, constructed from sample accession ERS3461322 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTGAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657298</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441524" alias="SC_EXP_30598_3#275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#275</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#275</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C18, constructed from sample accession ERS3461323 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCGCTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657299</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441525" alias="SC_EXP_30598_3#276">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#276</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#276</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D18, constructed from sample accession ERS3461324 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCCTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441526" alias="SC_EXP_30598_3#277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#277</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#277</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E18, constructed from sample accession ERS3461325 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTGCGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657301</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441527" alias="SC_EXP_30598_3#278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#278</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#278</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F18, constructed from sample accession ERS3461326 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AAAGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657302</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441528" alias="SC_EXP_30598_3#279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#279</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#279</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G18, constructed from sample accession ERS3461327 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCCGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461327">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441529" alias="SC_EXP_30598_3#280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#280</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#280</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H18, constructed from sample accession ERS3461328 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACTCGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441530" alias="SC_EXP_30598_3#281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#281</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I18, constructed from sample accession ERS3461329 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AACCGGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657305</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441531" alias="SC_EXP_30598_3#282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#282</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#282</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J18, constructed from sample accession ERS3461330 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGATTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441532" alias="SC_EXP_30598_3#283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#283</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#283</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K18, constructed from sample accession ERS3461331 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441533" alias="SC_EXP_30598_3#284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#284</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#284</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L18, constructed from sample accession ERS3461332 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTAAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657308</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441534" alias="SC_EXP_30598_3#285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#285</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M18, constructed from sample accession ERS3461333 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCTAGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657309</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441535" alias="SC_EXP_30598_3#286">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#286</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#286</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N18, constructed from sample accession ERS3461334 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCTTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657310</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441536" alias="SC_EXP_30598_3#287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#287</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#287</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O18, constructed from sample accession ERS3461335 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTATTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441537" alias="SC_EXP_30598_3#288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#288</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#288</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P18, constructed from sample accession ERS3461336 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441538" alias="SC_EXP_30598_3#289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#289</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#289</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A19, constructed from sample accession ERS3461337 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCGGAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657313</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441539" alias="SC_EXP_30598_3#290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#290</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#290</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B19, constructed from sample accession ERS3461338 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTGACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441540" alias="SC_EXP_30598_3#291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#291</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#291</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C19, constructed from sample accession ERS3461339 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTGGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657315</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441541" alias="SC_EXP_30598_3#292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#292</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#292</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D19, constructed from sample accession ERS3461340 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441542" alias="SC_EXP_30598_3#293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#293</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E19, constructed from sample accession ERS3461341 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTCAAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441543" alias="SC_EXP_30598_3#294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#294</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F19, constructed from sample accession ERS3461342 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657318</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441544" alias="SC_EXP_30598_3#295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#295</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G19, constructed from sample accession ERS3461343 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657319</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441545" alias="SC_EXP_30598_3#296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#296</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H19, constructed from sample accession ERS3461344 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441546" alias="SC_EXP_30598_3#297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#297</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I19, constructed from sample accession ERS3461345 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCTAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441547" alias="SC_EXP_30598_3#298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J19, constructed from sample accession ERS3461346 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCGTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657322</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441548" alias="SC_EXP_30598_3#299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K19, constructed from sample accession ERS3461347 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGAGGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441549" alias="SC_EXP_30598_3#300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L19, constructed from sample accession ERS3461348 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTAGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657324</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441550" alias="SC_EXP_30598_3#301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M19, constructed from sample accession ERS3461349 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGCGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657325</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441551" alias="SC_EXP_30598_3#302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N19, constructed from sample accession ERS3461350 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACGCGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441552" alias="SC_EXP_30598_3#303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#303</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O19, constructed from sample accession ERS3461351 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCGCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657327</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441553" alias="SC_EXP_30598_3#304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#304</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P19, constructed from sample accession ERS3461352 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657328</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441554" alias="SC_EXP_30598_3#305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#305</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A20, constructed from sample accession ERS3461353 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGTGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441555" alias="SC_EXP_30598_3#306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#306</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B20, constructed from sample accession ERS3461354 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441556" alias="SC_EXP_30598_3#307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#307</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C20, constructed from sample accession ERS3461355 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441557" alias="SC_EXP_30598_3#308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D20, constructed from sample accession ERS3461356 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441558" alias="SC_EXP_30598_3#309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E20, constructed from sample accession ERS3461357 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCAAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441559" alias="SC_EXP_30598_3#310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F20, constructed from sample accession ERS3461358 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence ACGTAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441560" alias="SC_EXP_30598_3#311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G20, constructed from sample accession ERS3461359 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCTATATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441561" alias="SC_EXP_30598_3#312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H20, constructed from sample accession ERS3461360 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTTCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657336</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441562" alias="SC_EXP_30598_3#313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I20, constructed from sample accession ERS3461361 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCTGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657337</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441563" alias="SC_EXP_30598_3#314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J20, constructed from sample accession ERS3461362 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGACCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657338</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441564" alias="SC_EXP_30598_3#315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#315</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K20, constructed from sample accession ERS3461363 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGTATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441565" alias="SC_EXP_30598_3#316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#316</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L20, constructed from sample accession ERS3461364 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441566" alias="SC_EXP_30598_3#317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#317</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M20, constructed from sample accession ERS3461365 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657341</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441567" alias="SC_EXP_30598_3#318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#318</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#318</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N20, constructed from sample accession ERS3461366 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGCAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657342</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441568" alias="SC_EXP_30598_3#319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O20, constructed from sample accession ERS3461367 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGGATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441569" alias="SC_EXP_30598_3#320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P20, constructed from sample accession ERS3461368 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGCGGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441570" alias="SC_EXP_30598_3#321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A21, constructed from sample accession ERS3461369 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657345</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441571" alias="SC_EXP_30598_3#322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B21, constructed from sample accession ERS3461370 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTTGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657346</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441572" alias="SC_EXP_30598_3#323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C21, constructed from sample accession ERS3461371 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCAGGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657347</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441573" alias="SC_EXP_30598_3#324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#324</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D21, constructed from sample accession ERS3461372 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441574" alias="SC_EXP_30598_3#325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#325</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E21, constructed from sample accession ERS3461373 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTGTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441575" alias="SC_EXP_30598_3#326">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#326</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#326</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F21, constructed from sample accession ERS3461374 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTTAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657350</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441576" alias="SC_EXP_30598_3#327">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#327</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#327</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G21, constructed from sample accession ERS3461375 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AAGGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441577" alias="SC_EXP_30598_3#328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#328</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#328</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H21, constructed from sample accession ERS3461376 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441578" alias="SC_EXP_30598_3#329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#329</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#329</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I21, constructed from sample accession ERS3461377 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTACTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441579" alias="SC_EXP_30598_3#330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#330</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#330</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J21, constructed from sample accession ERS3461378 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCACGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441580" alias="SC_EXP_30598_3#331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#331</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#331</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K21, constructed from sample accession ERS3461379 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCGAATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441581" alias="SC_EXP_30598_3#332">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#332</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#332</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L21, constructed from sample accession ERS3461380 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GATGAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441582" alias="SC_EXP_30598_3#333">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#333</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#333</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M21, constructed from sample accession ERS3461381 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTTTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441583" alias="SC_EXP_30598_3#334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#334</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#334</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N21, constructed from sample accession ERS3461382 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441584" alias="SC_EXP_30598_3#335">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#335</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#335</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O21, constructed from sample accession ERS3461383 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441585" alias="SC_EXP_30598_3#336">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#336</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#336</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P21, constructed from sample accession ERS3461384 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AACCTGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441586" alias="SC_EXP_30598_3#337">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#337</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#337</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A22, constructed from sample accession ERS3461385 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTTTCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441587" alias="SC_EXP_30598_3#338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#338</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#338</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B22, constructed from sample accession ERS3461386 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AAATGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441588" alias="SC_EXP_30598_3#339">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#339</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#339</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C22, constructed from sample accession ERS3461387 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CATCGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441589" alias="SC_EXP_30598_3#340">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#340</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#340</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D22, constructed from sample accession ERS3461388 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCACAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441590" alias="SC_EXP_30598_3#341">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#341</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#341</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E22, constructed from sample accession ERS3461389 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AGACTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441591" alias="SC_EXP_30598_3#342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#342</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#342</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F22, constructed from sample accession ERS3461390 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AATGCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441592" alias="SC_EXP_30598_3#343">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#343</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#343</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G22, constructed from sample accession ERS3461391 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GACGGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441593" alias="SC_EXP_30598_3#344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#344</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#344</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H22, constructed from sample accession ERS3461392 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGATAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461392">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441594" alias="SC_EXP_30598_3#345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#345</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#345</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I22, constructed from sample accession ERS3461393 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TAGGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441595" alias="SC_EXP_30598_3#346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#346</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#346</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J22, constructed from sample accession ERS3461394 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GAGCATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441596" alias="SC_EXP_30598_3#347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#347</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#347</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K22, constructed from sample accession ERS3461395 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441597" alias="SC_EXP_30598_3#348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#348</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#348</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L22, constructed from sample accession ERS3461396 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTCTTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441598" alias="SC_EXP_30598_3#349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#349</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#349</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M22, constructed from sample accession ERS3461397 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTAGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441599" alias="SC_EXP_30598_3#350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#350</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#350</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N22, constructed from sample accession ERS3461398 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGCCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657374</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441600" alias="SC_EXP_30598_3#351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#351</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#351</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O22, constructed from sample accession ERS3461399 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGGAGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441601" alias="SC_EXP_30598_3#352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#352</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#352</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P22, constructed from sample accession ERS3461400 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441602" alias="SC_EXP_30598_3#353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#353</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#353</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A23, constructed from sample accession ERS3461401 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTGAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441603" alias="SC_EXP_30598_3#354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#354</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#354</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B23, constructed from sample accession ERS3461402 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTTAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461402">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441604" alias="SC_EXP_30598_3#355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#355</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#355</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C23, constructed from sample accession ERS3461403 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTTGGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441605" alias="SC_EXP_30598_3#356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#356</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#356</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D23, constructed from sample accession ERS3461404 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441606" alias="SC_EXP_30598_3#357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#357</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#357</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E23, constructed from sample accession ERS3461405 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AACAGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461405">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441607" alias="SC_EXP_30598_3#358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#358</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#358</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F23, constructed from sample accession ERS3461406 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTTGTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461406">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441608" alias="SC_EXP_30598_3#359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#359</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#359</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G23, constructed from sample accession ERS3461407 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AATTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461407">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441609" alias="SC_EXP_30598_3#360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#360</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#360</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H23, constructed from sample accession ERS3461408 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence AAAGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657384</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441610" alias="SC_EXP_30598_3#361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#361</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#361</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I23, constructed from sample accession ERS3461409 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGCATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657385</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441611" alias="SC_EXP_30598_3#362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#362</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#362</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J23, constructed from sample accession ERS3461410 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TCAGTTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657386</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441612" alias="SC_EXP_30598_3#363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#363</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#363</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K23, constructed from sample accession ERS3461411 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGTTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657387</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441613" alias="SC_EXP_30598_3#364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#364</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#364</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L23, constructed from sample accession ERS3461412 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657388</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441614" alias="SC_EXP_30598_3#365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#365</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#365</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M23, constructed from sample accession ERS3461413 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGGGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657389</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441615" alias="SC_EXP_30598_3#366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#366</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#366</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N23, constructed from sample accession ERS3461414 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCAGCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441616" alias="SC_EXP_30598_3#367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#367</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#367</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O23, constructed from sample accession ERS3461415 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGTGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657391</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441617" alias="SC_EXP_30598_3#368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#368</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#368</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P23, constructed from sample accession ERS3461417 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGCCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441618" alias="SC_EXP_30598_3#369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#369</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#369</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:A24, constructed from sample accession ERS3461425 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGCACCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441619" alias="SC_EXP_30598_3#370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#370</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#370</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:B24, constructed from sample accession ERS3461426 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CCGATCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:B24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441620" alias="SC_EXP_30598_3#371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#371</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#371</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:C24, constructed from sample accession ERS3461427 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CAAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441621" alias="SC_EXP_30598_3#372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#372</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#372</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:D24, constructed from sample accession ERS3461428 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GGCGTCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:D24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441622" alias="SC_EXP_30598_3#373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#373</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#373</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:E24, constructed from sample accession ERS3461429 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTAGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441623" alias="SC_EXP_30598_3#374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#374</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#374</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:F24, constructed from sample accession ERS3461430 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GTCGGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:F24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441624" alias="SC_EXP_30598_3#375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#375</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#375</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:G24, constructed from sample accession ERS3461431 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCCTCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657407</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441625" alias="SC_EXP_30598_3#376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#376</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#376</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:H24, constructed from sample accession ERS3461432 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTATACCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:H24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441626" alias="SC_EXP_30598_3#377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#377</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#377</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:I24, constructed from sample accession ERS3461433 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TGGTCGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441627" alias="SC_EXP_30598_3#378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#378</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#378</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:J24, constructed from sample accession ERS3461434 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTAAACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:J24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441628" alias="SC_EXP_30598_3#379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#379</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#379</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:K24, constructed from sample accession ERS3461435 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CGTTGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441629" alias="SC_EXP_30598_3#380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#380</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#380</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:L24, constructed from sample accession ERS3461436 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CACTCTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:L24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441630" alias="SC_EXP_30598_3#381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#381</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#381</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:M24, constructed from sample accession ERS3461437 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TTGTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441631" alias="SC_EXP_30598_3#382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#382</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#382</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:N24, constructed from sample accession ERS3461438 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence GCAGCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:N24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441632" alias="SC_EXP_30598_3#383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#383</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#383</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:O24, constructed from sample accession ERS3461439 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence CTGCCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4441633" alias="SC_EXP_30598_3#384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4441633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30598_3#384</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30598_3#384</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP104882">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP104882</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB23147</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN571468O:P24, constructed from sample accession ERS3461440 for study accession ERP104882.  This is part of an Illumina multiplexed sequencing run (30598_3).  This submission includes reads tagged with the sequence TACCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3461440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3461440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5657416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN571468O:P24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="600"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>scRNA 384</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
