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  <EXPERIMENT accession="ERX10489374" alias="SC_EXP_44188_1#1" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489374</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A1, constructed from sample accession ERS8066010 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="512" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489375" alias="SC_EXP_44188_1#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489375</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B1, constructed from sample accession ERS8066018 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="524" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489376" alias="SC_EXP_44188_1#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489376</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C1, constructed from sample accession ERS8066035 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTTCGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066035">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489377" alias="SC_EXP_44188_1#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489377</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D1, constructed from sample accession ERS8066036 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CTCATATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="537" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489378" alias="SC_EXP_44188_1#5" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489378</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E1, constructed from sample accession ERS8066037 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGTTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066037">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="516" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489379" alias="SC_EXP_44188_1#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489379</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F1, constructed from sample accession ERS8065970 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTCGATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="546" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489380" alias="SC_EXP_44188_1#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489380</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G1, constructed from sample accession ERS8065971 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GAGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417095</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="547" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489381" alias="SC_EXP_44188_1#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489381</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H1, constructed from sample accession ERS8065972 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065972">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="159"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489382" alias="SC_EXP_44188_1#9" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489382</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A2, constructed from sample accession ERS8065973 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GACTATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065973">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489383" alias="SC_EXP_44188_1#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489383</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B2, constructed from sample accession ERS8065975 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CGTCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="534" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489384" alias="SC_EXP_44188_1#11" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489384</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C2, constructed from sample accession ERS8065978 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTCAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065978">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="519" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489385" alias="SC_EXP_44188_1#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489385</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D2, constructed from sample accession ERS8065980 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TCGGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="529" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489386" alias="SC_EXP_44188_1#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489386</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E2, constructed from sample accession ERS8065983 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTCCTGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="546" NOMINAL_SDEV="143"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489387" alias="SC_EXP_44188_1#14" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489387</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F2, constructed from sample accession ERS8065984 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGCTAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="153"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489388" alias="SC_EXP_44188_1#15" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489388</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G2, constructed from sample accession ERS8065986 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CTCCAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489389" alias="SC_EXP_44188_1#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489389</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H2, constructed from sample accession ERS8065985 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GATTAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="531" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489390" alias="SC_EXP_44188_1#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489390</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A3, constructed from sample accession ERS8065987 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence ACGCCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="504" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489391" alias="SC_EXP_44188_1#18" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489391</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B3, constructed from sample accession ERS8065988 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TCCTATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="550" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489392" alias="SC_EXP_44188_1#19" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489392</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C3, constructed from sample accession ERS8065990 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065990">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="492" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489393" alias="SC_EXP_44188_1#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489393</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D3, constructed from sample accession ERS8065991 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TACGGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="506" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489394" alias="SC_EXP_44188_1#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489394</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E3, constructed from sample accession ERS8065993 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="539" NOMINAL_SDEV="121"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489395" alias="SC_EXP_44188_1#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489395</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F3, constructed from sample accession ERS8066001 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TGGGTTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066001">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066001</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="140"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489396" alias="SC_EXP_44188_1#23" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489396</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G3, constructed from sample accession ERS8065998 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence AGATCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065998">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065998</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="54"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489397" alias="SC_EXP_44188_1#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489397</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H3, constructed from sample accession ERS8066005 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GCGTACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066005">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="523" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489398" alias="SC_EXP_44188_1#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489398</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A4, constructed from sample accession ERS8066007 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CCATCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066007">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066007</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="507" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489399" alias="SC_EXP_44188_1#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489399</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B4, constructed from sample accession ERS8066050 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTCGGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066050">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="505" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489400" alias="SC_EXP_44188_1#27" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489400</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C4, constructed from sample accession ERS8066052 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TGCAAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489401" alias="SC_EXP_44188_1#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489401</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D4, constructed from sample accession ERS8066051 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTCAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066051">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="539" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489402" alias="SC_EXP_44188_1#29" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489402</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E4, constructed from sample accession ERS8066009 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CGCGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066009">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="541" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489403" alias="SC_EXP_44188_1#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489403</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F4, constructed from sample accession ERS8066008 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGCGGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="539" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489404" alias="SC_EXP_44188_1#31" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489404</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G4, constructed from sample accession ERS8066011 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTTTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="143"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489405" alias="SC_EXP_44188_1#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489405</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H4, constructed from sample accession ERS8066012 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CTAGATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066012">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="525" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489406" alias="SC_EXP_44188_1#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489406</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A5, constructed from sample accession ERS8066013 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CCGGGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066013">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489407" alias="SC_EXP_44188_1#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489407</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B5, constructed from sample accession ERS8066017 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence ACGTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066017">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="528" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489408" alias="SC_EXP_44188_1#35" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489408</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C5, constructed from sample accession ERS8066015 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CGGTATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="541" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489409" alias="SC_EXP_44188_1#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489409</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D5, constructed from sample accession ERS8066014 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTCGTTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489410" alias="SC_EXP_44188_1#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489410</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E5, constructed from sample accession ERS8066016 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TGCTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="522" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489411" alias="SC_EXP_44188_1#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489411</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F5, constructed from sample accession ERS8066019 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TGTCGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066019">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="498" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489412" alias="SC_EXP_44188_1#39" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489412</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G5, constructed from sample accession ERS8066020 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CTTTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066020">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066020</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="534" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489413" alias="SC_EXP_44188_1#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489413</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H5, constructed from sample accession ERS8066021 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence AACCAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="535" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489414" alias="SC_EXP_44188_1#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489414</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A6, constructed from sample accession ERS8066022 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTTGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066022">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="534" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489415" alias="SC_EXP_44188_1#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489415</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B6, constructed from sample accession ERS8066024 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CCAAAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489416" alias="SC_EXP_44188_1#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489416</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C6, constructed from sample accession ERS8066025 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GCCTTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066025">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489417" alias="SC_EXP_44188_1#44" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489417</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D6, constructed from sample accession ERS8066023 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CAGGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066023">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="529" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489418" alias="SC_EXP_44188_1#45" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489418</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E6, constructed from sample accession ERS8066026 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GCGGGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066026">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="533" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489419" alias="SC_EXP_44188_1#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489419</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F6, constructed from sample accession ERS8066028 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CCTGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066028">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489420" alias="SC_EXP_44188_1#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489420</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G6, constructed from sample accession ERS8066029 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGCCGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="508" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489421" alias="SC_EXP_44188_1#48" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489421</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H6, constructed from sample accession ERS8066027 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CAAATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489422" alias="SC_EXP_44188_1#49" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489422</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A7, constructed from sample accession ERS8066030 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CAATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="511" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489423" alias="SC_EXP_44188_1#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489423</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B7, constructed from sample accession ERS8066031 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTCCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066031">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="528" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489424" alias="SC_EXP_44188_1#51" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489424</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C7, constructed from sample accession ERS8066033 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CCGGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="540" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489425" alias="SC_EXP_44188_1#52" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489425</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D7, constructed from sample accession ERS8066032 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTCGGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489426" alias="SC_EXP_44188_1#53" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489426</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E7, constructed from sample accession ERS8066034 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTTAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066034">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="552" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489427" alias="SC_EXP_44188_1#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489427</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F7, constructed from sample accession ERS8066038 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence AACGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066038">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="507" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489428" alias="SC_EXP_44188_1#55" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489428</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G7, constructed from sample accession ERS8066039 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGAGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489429" alias="SC_EXP_44188_1#56" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489429</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H7, constructed from sample accession ERS8066041 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTTGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066041">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="522" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489430" alias="SC_EXP_44188_1#57" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489430</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A8, constructed from sample accession ERS8066040 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TCTTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066040">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="513" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489431" alias="SC_EXP_44188_1#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489431</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B8, constructed from sample accession ERS8066042 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TGGCCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="532" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489432" alias="SC_EXP_44188_1#59" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489432</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C8, constructed from sample accession ERS8066043 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TCTGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="531" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489433" alias="SC_EXP_44188_1#60" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489433</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D8, constructed from sample accession ERS8066044 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TCGGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066044">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="529" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489434" alias="SC_EXP_44188_1#61" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489434</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E8, constructed from sample accession ERS8066045 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TGTGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066045">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="535" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489435" alias="SC_EXP_44188_1#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489435</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F8, constructed from sample accession ERS8066046 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CGACGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="532" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489436" alias="SC_EXP_44188_1#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489436</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G8, constructed from sample accession ERS8066048 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTAAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066048">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="542" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489437" alias="SC_EXP_44188_1#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489437</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H8, constructed from sample accession ERS8066047 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CCTTCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="535" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489438" alias="SC_EXP_44188_1#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489438</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A9, constructed from sample accession ERS8066049 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTTGAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="519" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489439" alias="SC_EXP_44188_1#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489439</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B9, constructed from sample accession ERS8065963 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGCCTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="522" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489440" alias="SC_EXP_44188_1#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489440</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C9, constructed from sample accession ERS8065964 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence AAAGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="530" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489441" alias="SC_EXP_44188_1#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489441</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D9, constructed from sample accession ERS8065966 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence ACTCGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="531" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489442" alias="SC_EXP_44188_1#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489442</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E9, constructed from sample accession ERS8065968 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CGATTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417092</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="535" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489443" alias="SC_EXP_44188_1#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489443</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F9, constructed from sample accession ERS8065965 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTAAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="528" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489444" alias="SC_EXP_44188_1#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489444</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G9, constructed from sample accession ERS8065969 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTCTTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417093</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="534" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489445" alias="SC_EXP_44188_1#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489445</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H9, constructed from sample accession ERS8065974 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CGTGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489446" alias="SC_EXP_44188_1#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489446</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A10, constructed from sample accession ERS8065976 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CACTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065976">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="516" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489447" alias="SC_EXP_44188_1#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489447</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B10, constructed from sample accession ERS8065977 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTGTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="529" NOMINAL_SDEV="127"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489448" alias="SC_EXP_44188_1#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489448</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C10, constructed from sample accession ERS8065979 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence ACGTAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065979">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489449" alias="SC_EXP_44188_1#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489449</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D10, constructed from sample accession ERS8065981 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CTTTCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065981">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="522" NOMINAL_SDEV="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489450" alias="SC_EXP_44188_1#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489450</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E10, constructed from sample accession ERS8065982 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTGACCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065982">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489451" alias="SC_EXP_44188_1#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489451</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F10, constructed from sample accession ERS8065989 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTCCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489452" alias="SC_EXP_44188_1#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489452</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G10, constructed from sample accession ERS8065992 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GTGCAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065992">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065992</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="512" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489453" alias="SC_EXP_44188_1#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489453</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H10, constructed from sample accession ERS8065994 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TGCGGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489454" alias="SC_EXP_44188_1#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489454</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A11, constructed from sample accession ERS8065995 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence AAATGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="520" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489455" alias="SC_EXP_44188_1#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489455</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B11, constructed from sample accession ERS8065996 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TCACAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489456" alias="SC_EXP_44188_1#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489456</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:C11, constructed from sample accession ERS8065997 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence AATGCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="529" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489457" alias="SC_EXP_44188_1#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489457</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:D11, constructed from sample accession ERS8066000 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CGATAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="41"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489458" alias="SC_EXP_44188_1#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489458</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:E11, constructed from sample accession ERS8065999 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GAGCATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8065999">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8065999</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="495" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489459" alias="SC_EXP_44188_1#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489459</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:F11, constructed from sample accession ERS8066002 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence TTCTTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066002">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066002</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489460" alias="SC_EXP_44188_1#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489460</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:G11, constructed from sample accession ERS8066003 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGGCCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066003">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="512" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489461" alias="SC_EXP_44188_1#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489461</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:H11, constructed from sample accession ERS8066004 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066004">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066004</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="498" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489462" alias="SC_EXP_44188_1#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489462</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:A12, constructed from sample accession ERS8066006 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence CCGATCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="515" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489463" alias="SC_EXP_44188_1#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489463</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_1#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882192J:B12, constructed from sample accession ERS8066053 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_1).  This submission includes reads tagged with the sequence GGCGTCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS8066053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS8066053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA10417178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882192J:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="520" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489464" alias="SC_EXP_44188_3#1" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489464</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A1, constructed from sample accession ERS9756301 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGGATCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="581" NOMINAL_SDEV="149"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489465" alias="SC_EXP_44188_3#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489465</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B1, constructed from sample accession ERS9756308 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GATACTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="500" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489466" alias="SC_EXP_44188_3#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489466</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C1, constructed from sample accession ERS9756316 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCCAAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="530" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489467" alias="SC_EXP_44188_3#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489467</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D1, constructed from sample accession ERS9756328 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGCGGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109493</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="171"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489468" alias="SC_EXP_44188_3#5" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489468</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E1, constructed from sample accession ERS9756344 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCCTTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="555" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489469" alias="SC_EXP_44188_3#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489469</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F1, constructed from sample accession ERS9756362 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCACTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="549" NOMINAL_SDEV="118"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489470" alias="SC_EXP_44188_3#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489470</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G1, constructed from sample accession ERS9756373 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGCACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109538</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="69"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489471" alias="SC_EXP_44188_3#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489471</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H1, constructed from sample accession ERS9756377 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGCGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109542</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="541" NOMINAL_SDEV="149"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489472" alias="SC_EXP_44188_3#9" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489472</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A2, constructed from sample accession ERS9756378 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGGCTTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109543</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="54"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489473" alias="SC_EXP_44188_3#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489473</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B2, constructed from sample accession ERS9756379 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GAGTGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109544</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489474" alias="SC_EXP_44188_3#11" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489474</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C2, constructed from sample accession ERS9756382 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CACAAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109547</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="559" NOMINAL_SDEV="143"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489475" alias="SC_EXP_44188_3#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489475</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D2, constructed from sample accession ERS9756386 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTAACACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="520" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489476" alias="SC_EXP_44188_3#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489476</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E2, constructed from sample accession ERS9756387 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence AGCGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418" NOMINAL_SDEV="64"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489477" alias="SC_EXP_44188_3#14" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489477</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F2, constructed from sample accession ERS9756391 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GTCACGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109556</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489478" alias="SC_EXP_44188_3#15" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489478</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G2, constructed from sample accession ERS9756396 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CAACCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109561</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489479" alias="SC_EXP_44188_3#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489479</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H2, constructed from sample accession ERS9756397 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CATGGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109562</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="553" NOMINAL_SDEV="157"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489480" alias="SC_EXP_44188_3#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489480</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A3, constructed from sample accession ERS9756399 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGATTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109564</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="550" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489481" alias="SC_EXP_44188_3#18" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489481</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B3, constructed from sample accession ERS9756405 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence AACTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756405">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109572</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489482" alias="SC_EXP_44188_3#19" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489482</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C3, constructed from sample accession ERS9756478 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence AAACGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="540" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489483" alias="SC_EXP_44188_3#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489483</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D3, constructed from sample accession ERS9756480 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCTCGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756480">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756480</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="537" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489484" alias="SC_EXP_44188_3#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489484</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E3, constructed from sample accession ERS9756417 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGTCGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109582</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489485" alias="SC_EXP_44188_3#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489485</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F3, constructed from sample accession ERS9756419 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCACGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489486" alias="SC_EXP_44188_3#23" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489486</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G3, constructed from sample accession ERS9756422 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGGGCTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109587</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489487" alias="SC_EXP_44188_3#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489487</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H3, constructed from sample accession ERS9756296 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCTGTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489488" alias="SC_EXP_44188_3#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489488</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A4, constructed from sample accession ERS9756298 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GTGCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489489" alias="SC_EXP_44188_3#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489489</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B4, constructed from sample accession ERS9756297 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGCTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756297">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="544" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489490" alias="SC_EXP_44188_3#27" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489490</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C4, constructed from sample accession ERS9756299 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CAGAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489491" alias="SC_EXP_44188_3#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489491</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D4, constructed from sample accession ERS9756303 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GAAACCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="552" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489492" alias="SC_EXP_44188_3#29" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489492</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E4, constructed from sample accession ERS9756300 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGAGACCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418" NOMINAL_SDEV="62"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489493" alias="SC_EXP_44188_3#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489493</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F4, constructed from sample accession ERS9756302 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGCAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="504" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489494" alias="SC_EXP_44188_3#31" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489494</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G4, constructed from sample accession ERS9756304 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TCCGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="34"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489495" alias="SC_EXP_44188_3#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489495</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H4, constructed from sample accession ERS9756305 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GTTTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489496" alias="SC_EXP_44188_3#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489496</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A5, constructed from sample accession ERS9756307 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CTCTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="559" NOMINAL_SDEV="165"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489497" alias="SC_EXP_44188_3#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489497</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B5, constructed from sample accession ERS9756306 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GAGAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="524" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489498" alias="SC_EXP_44188_3#35" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489498</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C5, constructed from sample accession ERS9756310 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGAAACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489499" alias="SC_EXP_44188_3#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489499</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D5, constructed from sample accession ERS9756309 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TCCATTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="556" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489500" alias="SC_EXP_44188_3#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489500</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E5, constructed from sample accession ERS9756311 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CCTAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="551" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489501" alias="SC_EXP_44188_3#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489501</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F5, constructed from sample accession ERS9756312 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTCCAAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="500" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489502" alias="SC_EXP_44188_3#39" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489502</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G5, constructed from sample accession ERS9756313 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence ACTGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489503" alias="SC_EXP_44188_3#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489503</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H5, constructed from sample accession ERS9756314 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGAGGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489504" alias="SC_EXP_44188_3#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489504</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A6, constructed from sample accession ERS9756315 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTTAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="546" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489505" alias="SC_EXP_44188_3#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489505</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B6, constructed from sample accession ERS9756317 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CAAAGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756317">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="423" NOMINAL_SDEV="55"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489506" alias="SC_EXP_44188_3#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489506</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C6, constructed from sample accession ERS9756318 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence AGACGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="542" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489507" alias="SC_EXP_44188_3#44" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489507</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D6, constructed from sample accession ERS9756319 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGAAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="523" NOMINAL_SDEV="140"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489508" alias="SC_EXP_44188_3#45" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489508</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E6, constructed from sample accession ERS9756321 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTCCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489509" alias="SC_EXP_44188_3#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489509</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F6, constructed from sample accession ERS9756320 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGGTTGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="512" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489510" alias="SC_EXP_44188_3#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489510</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G6, constructed from sample accession ERS9756322 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TCCTTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489511" alias="SC_EXP_44188_3#48" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489511</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H6, constructed from sample accession ERS9756323 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CAGAAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="31"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489512" alias="SC_EXP_44188_3#49" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489512</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A7, constructed from sample accession ERS9756324 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CTGAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489513" alias="SC_EXP_44188_3#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489513</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B7, constructed from sample accession ERS9756327 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGTTGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756327">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="539" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489514" alias="SC_EXP_44188_3#51" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489514</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C7, constructed from sample accession ERS9756325 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGGGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="491" NOMINAL_SDEV="121"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489515" alias="SC_EXP_44188_3#52" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489515</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D7, constructed from sample accession ERS9756326 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GACGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="535" NOMINAL_SDEV="146"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489516" alias="SC_EXP_44188_3#53" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489516</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E7, constructed from sample accession ERS9756329 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGCTTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489517" alias="SC_EXP_44188_3#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489517</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F7, constructed from sample accession ERS9756330 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGTTCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489518" alias="SC_EXP_44188_3#55" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489518</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G7, constructed from sample accession ERS9756331 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GAGCACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="500" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489519" alias="SC_EXP_44188_3#56" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489519</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H7, constructed from sample accession ERS9756332 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489520" alias="SC_EXP_44188_3#57" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489520</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A8, constructed from sample accession ERS9756333 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GAGGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109498</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="550" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489521" alias="SC_EXP_44188_3#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489521</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B8, constructed from sample accession ERS9756334 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CCTCACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="544" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489522" alias="SC_EXP_44188_3#59" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489522</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C8, constructed from sample accession ERS9756336 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGGCTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="532" NOMINAL_SDEV="147"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489523" alias="SC_EXP_44188_3#60" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489523</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D8, constructed from sample accession ERS9756335 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCTCTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="553" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489524" alias="SC_EXP_44188_3#61" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489524</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E8, constructed from sample accession ERS9756337 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGGCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489525" alias="SC_EXP_44188_3#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489525</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F8, constructed from sample accession ERS9756338 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TCGCATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="542" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489526" alias="SC_EXP_44188_3#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489526</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G8, constructed from sample accession ERS9756339 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGGCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489527" alias="SC_EXP_44188_3#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489527</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H8, constructed from sample accession ERS9756340 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGTCTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="58"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489528" alias="SC_EXP_44188_3#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489528</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A9, constructed from sample accession ERS9756341 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GTGGCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="519" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489529" alias="SC_EXP_44188_3#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489529</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B9, constructed from sample accession ERS9756343 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TCGCTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="153"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489530" alias="SC_EXP_44188_3#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489530</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C9, constructed from sample accession ERS9756342 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTGCGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489531" alias="SC_EXP_44188_3#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489531</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D9, constructed from sample accession ERS9756345 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGCCGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109510</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="548" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489532" alias="SC_EXP_44188_3#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489532</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E9, constructed from sample accession ERS9756346 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence AACCGGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109511</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="553" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489533" alias="SC_EXP_44188_3#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489533</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F9, constructed from sample accession ERS9756347 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGTTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="543" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489534" alias="SC_EXP_44188_3#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489534</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G9, constructed from sample accession ERS9756348 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCTAGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489535" alias="SC_EXP_44188_3#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489535</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H9, constructed from sample accession ERS9756349 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTATTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109514</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="531" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489536" alias="SC_EXP_44188_3#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489536</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A10, constructed from sample accession ERS9756350 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GTGTGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489537" alias="SC_EXP_44188_3#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489537</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B10, constructed from sample accession ERS9756351 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGGTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109516</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489538" alias="SC_EXP_44188_3#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489538</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C10, constructed from sample accession ERS9756352 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CCAAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109517</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489539" alias="SC_EXP_44188_3#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489539</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D10, constructed from sample accession ERS9756354 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TCTATATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489540" alias="SC_EXP_44188_3#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489540</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E10, constructed from sample accession ERS9756353 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CCTGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="559" NOMINAL_SDEV="143"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489541" alias="SC_EXP_44188_3#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489541</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F10, constructed from sample accession ERS9756355 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CTGTATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489542" alias="SC_EXP_44188_3#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489542</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G10, constructed from sample accession ERS9756356 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CATAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="64"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489543" alias="SC_EXP_44188_3#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489543</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H10, constructed from sample accession ERS9756357 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGCATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489544" alias="SC_EXP_44188_3#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489544</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A11, constructed from sample accession ERS9756358 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GTTTCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="569" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489545" alias="SC_EXP_44188_3#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489545</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B11, constructed from sample accession ERS9756359 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CATCGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="537" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489546" alias="SC_EXP_44188_3#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489546</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C11, constructed from sample accession ERS9756360 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence AGACTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="533" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489547" alias="SC_EXP_44188_3#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489547</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D11, constructed from sample accession ERS9756361 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GACGGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489548" alias="SC_EXP_44188_3#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489548</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E11, constructed from sample accession ERS9756363 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TAGGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489549" alias="SC_EXP_44188_3#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489549</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F11, constructed from sample accession ERS9756364 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTTCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="534" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489550" alias="SC_EXP_44188_3#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489550</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G11, constructed from sample accession ERS9756365 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CTAGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489551" alias="SC_EXP_44188_3#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489551</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H11, constructed from sample accession ERS9756366 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GGGAGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109531</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="555" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489552" alias="SC_EXP_44188_3#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489552</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:A12, constructed from sample accession ERS9756367 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGCACCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="529" NOMINAL_SDEV="153"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489553" alias="SC_EXP_44188_3#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489553</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:B12, constructed from sample accession ERS9756368 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CAAAGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="504" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489554" alias="SC_EXP_44188_3#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489554</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:C12, constructed from sample accession ERS9756369 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GTAGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489555" alias="SC_EXP_44188_3#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489555</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:D12, constructed from sample accession ERS9756370 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence GCCTCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="548" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489556" alias="SC_EXP_44188_3#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489556</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:E12, constructed from sample accession ERS9756374 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TGGTCGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109539</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="505" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489557" alias="SC_EXP_44188_3#94" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489557</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:F12, constructed from sample accession ERS9756371 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CGTTGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489558" alias="SC_EXP_44188_3#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489558</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:G12, constructed from sample accession ERS9756372 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence TTGTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109537</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="543" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489559" alias="SC_EXP_44188_3#96" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489559</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_3#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881838U:H12, constructed from sample accession ERS9756375 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_3).  This submission includes reads tagged with the sequence CTGCCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109540</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881838U:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="566" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489560" alias="SC_EXP_44188_4#1" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489560</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A1, constructed from sample accession ERS9756376 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109541</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="551" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489561" alias="SC_EXP_44188_4#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489561</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B1, constructed from sample accession ERS9756380 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109545</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489562" alias="SC_EXP_44188_4#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489562</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C1, constructed from sample accession ERS9756381 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTTCGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109546</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489563" alias="SC_EXP_44188_4#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489563</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D1, constructed from sample accession ERS9756383 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CTCATATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489564" alias="SC_EXP_44188_4#5" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489564</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E1, constructed from sample accession ERS9756384 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGTTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489565" alias="SC_EXP_44188_4#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489565</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F1, constructed from sample accession ERS9756385 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTCGATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="500" NOMINAL_SDEV="153"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489566" alias="SC_EXP_44188_4#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489566</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G1, constructed from sample accession ERS9756388 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GAGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="485" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489567" alias="SC_EXP_44188_4#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489567</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H1, constructed from sample accession ERS9756389 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="507" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489568" alias="SC_EXP_44188_4#9" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489568</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A2, constructed from sample accession ERS9756390 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GACTATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109555</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489569" alias="SC_EXP_44188_4#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489569</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B2, constructed from sample accession ERS9756393 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CGTCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109557</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="507" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489570" alias="SC_EXP_44188_4#11" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489570</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C2, constructed from sample accession ERS9756392 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTCAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756392">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109558</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="524" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489571" alias="SC_EXP_44188_4#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489571</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D2, constructed from sample accession ERS9756394 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TCGGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109559</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="516" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489572" alias="SC_EXP_44188_4#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489572</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E2, constructed from sample accession ERS9756395 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTCCTGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109560</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489573" alias="SC_EXP_44188_4#14" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489573</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F2, constructed from sample accession ERS9756398 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGCTAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109563</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="507" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489574" alias="SC_EXP_44188_4#15" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489574</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G2, constructed from sample accession ERS9756400 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CTCCAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109565</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="539" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489575" alias="SC_EXP_44188_4#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489575</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H2, constructed from sample accession ERS9756401 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GATTAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109566</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="533" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489576" alias="SC_EXP_44188_4#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489576</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A3, constructed from sample accession ERS9756402 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence ACGCCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756402">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489577" alias="SC_EXP_44188_4#18" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489577</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B3, constructed from sample accession ERS9756403 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TCCTATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="525" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489578" alias="SC_EXP_44188_4#19" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489578</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C3, constructed from sample accession ERS9756404 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489579" alias="SC_EXP_44188_4#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489579</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D3, constructed from sample accession ERS9756407 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TACGGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756407">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109570</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489580" alias="SC_EXP_44188_4#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489580</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E3, constructed from sample accession ERS9756406 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756406">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489581" alias="SC_EXP_44188_4#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489581</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F3, constructed from sample accession ERS9756408 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TGGGTTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109573</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489582" alias="SC_EXP_44188_4#23" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489582</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G3, constructed from sample accession ERS9756464 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence AGATCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756464">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489583" alias="SC_EXP_44188_4#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489583</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H3, constructed from sample accession ERS9756465 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GCGTACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756465">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489584" alias="SC_EXP_44188_4#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489584</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A4, constructed from sample accession ERS9756466 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CCATCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756466">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489585" alias="SC_EXP_44188_4#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489585</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B4, constructed from sample accession ERS9756467 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTCGGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756467">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="63"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489586" alias="SC_EXP_44188_4#27" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489586</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C4, constructed from sample accession ERS9756468 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TGCAAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756468">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489587" alias="SC_EXP_44188_4#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489587</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D4, constructed from sample accession ERS9756469 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTCAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756469">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="62"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489588" alias="SC_EXP_44188_4#29" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489588</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E4, constructed from sample accession ERS9756470 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CGCGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756470">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756470</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489589" alias="SC_EXP_44188_4#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489589</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F4, constructed from sample accession ERS9756471 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGCGGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756471">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756471</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489590" alias="SC_EXP_44188_4#31" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489590</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G4, constructed from sample accession ERS9756472 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTTTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756472">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="516" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489591" alias="SC_EXP_44188_4#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489591</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H4, constructed from sample accession ERS9756473 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CTAGATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756473">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489592" alias="SC_EXP_44188_4#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489592</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A5, constructed from sample accession ERS9756474 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CCGGGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756474">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="506" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489593" alias="SC_EXP_44188_4#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489593</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B5, constructed from sample accession ERS9756475 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence ACGTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756475">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756475</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="522" NOMINAL_SDEV="127"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489594" alias="SC_EXP_44188_4#35" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489594</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C5, constructed from sample accession ERS9756476 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CGGTATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756476">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756476</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="505" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489595" alias="SC_EXP_44188_4#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489595</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D5, constructed from sample accession ERS9756477 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTCGTTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756477">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756477</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="494" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489596" alias="SC_EXP_44188_4#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489596</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E5, constructed from sample accession ERS9756479 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TGCTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756479">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756479</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489597" alias="SC_EXP_44188_4#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489597</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F5, constructed from sample accession ERS9756481 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TGTCGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756481">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756481</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="512" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489598" alias="SC_EXP_44188_4#39" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489598</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G5, constructed from sample accession ERS9756482 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CTTTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756482">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756482</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="523" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489599" alias="SC_EXP_44188_4#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489599</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H5, constructed from sample accession ERS9756483 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence AACCAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756483">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756483</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109648</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="491" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489600" alias="SC_EXP_44188_4#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489600</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A6, constructed from sample accession ERS9756484 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTTGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756484">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756484</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109649</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489601" alias="SC_EXP_44188_4#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489601</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B6, constructed from sample accession ERS9756485 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CCAAAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756485">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756485</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489602" alias="SC_EXP_44188_4#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489602</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C6, constructed from sample accession ERS9756486 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GCCTTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756486">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756486</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="504" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489603" alias="SC_EXP_44188_4#44" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489603</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D6, constructed from sample accession ERS9756487 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CAGGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756487">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756487</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="523" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489604" alias="SC_EXP_44188_4#45" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489604</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E6, constructed from sample accession ERS9756409 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GCGGGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109574</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489605" alias="SC_EXP_44188_4#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489605</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F6, constructed from sample accession ERS9756410 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CCTGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109575</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="530" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489606" alias="SC_EXP_44188_4#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489606</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G6, constructed from sample accession ERS9756411 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGCCGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109576</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489607" alias="SC_EXP_44188_4#48" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489607</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H6, constructed from sample accession ERS9756412 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CAAATCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109577</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="486" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489608" alias="SC_EXP_44188_4#49" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489608</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A7, constructed from sample accession ERS9756413 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CAATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109578</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="508" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489609" alias="SC_EXP_44188_4#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489609</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B7, constructed from sample accession ERS9756414 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTCCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109579</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489610" alias="SC_EXP_44188_4#51" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489610</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C7, constructed from sample accession ERS9756416 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CCGGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109580</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489611" alias="SC_EXP_44188_4#52" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489611</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D7, constructed from sample accession ERS9756415 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTCGGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109581</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489612" alias="SC_EXP_44188_4#53" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489612</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E7, constructed from sample accession ERS9756418 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTTAATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109583</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489613" alias="SC_EXP_44188_4#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489613</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F7, constructed from sample accession ERS9756420 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence AACGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109584</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489614" alias="SC_EXP_44188_4#55" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489614</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G7, constructed from sample accession ERS9756421 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGAGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109586</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489615" alias="SC_EXP_44188_4#56" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489615</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H7, constructed from sample accession ERS9756424 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTTGTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="446" NOMINAL_SDEV="64"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489616" alias="SC_EXP_44188_4#57" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489616</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A8, constructed from sample accession ERS9756423 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TCTTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="535" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489617" alias="SC_EXP_44188_4#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489617</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B8, constructed from sample accession ERS9756425 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TGGCCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="64"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489618" alias="SC_EXP_44188_4#59" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489618</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C8, constructed from sample accession ERS9756426 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TCTGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489619" alias="SC_EXP_44188_4#60" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489619</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D8, constructed from sample accession ERS9756427 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TCGGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="55"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489620" alias="SC_EXP_44188_4#61" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489620</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E8, constructed from sample accession ERS9756428 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TGTGGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109593</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="537" NOMINAL_SDEV="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489621" alias="SC_EXP_44188_4#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489621</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F8, constructed from sample accession ERS9756429 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CGACGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489622" alias="SC_EXP_44188_4#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489622</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G8, constructed from sample accession ERS9756430 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTAAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="525" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489623" alias="SC_EXP_44188_4#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489623</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H8, constructed from sample accession ERS9756431 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CCTTCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489624" alias="SC_EXP_44188_4#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489624</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A9, constructed from sample accession ERS9756432 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTTGAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489625" alias="SC_EXP_44188_4#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489625</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B9, constructed from sample accession ERS9756433 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGCCTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="529" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489626" alias="SC_EXP_44188_4#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489626</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C9, constructed from sample accession ERS9756434 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence AAAGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="506" NOMINAL_SDEV="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489627" alias="SC_EXP_44188_4#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489627</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D9, constructed from sample accession ERS9756435 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence ACTCGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="518" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489628" alias="SC_EXP_44188_4#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489628</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E9, constructed from sample accession ERS9756436 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CGATTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="548" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489629" alias="SC_EXP_44188_4#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489629</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F9, constructed from sample accession ERS9756437 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTAAGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489630" alias="SC_EXP_44188_4#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489630</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G9, constructed from sample accession ERS9756438 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTCTTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="515" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489631" alias="SC_EXP_44188_4#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489631</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H9, constructed from sample accession ERS9756439 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CGTGGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109604</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489632" alias="SC_EXP_44188_4#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489632</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A10, constructed from sample accession ERS9756440 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CACTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="522" NOMINAL_SDEV="127"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489633" alias="SC_EXP_44188_4#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489633</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B10, constructed from sample accession ERS9756441 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTGTCGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756441">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109606</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489634" alias="SC_EXP_44188_4#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489634</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C10, constructed from sample accession ERS9756442 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence ACGTAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109607</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489635" alias="SC_EXP_44188_4#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489635</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D10, constructed from sample accession ERS9756443 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CTTTCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756443">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489636" alias="SC_EXP_44188_4#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489636</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E10, constructed from sample accession ERS9756446 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTGACCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756446">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109612</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489637" alias="SC_EXP_44188_4#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489637</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F10, constructed from sample accession ERS9756444 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTCCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756444">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109609</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="532" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489638" alias="SC_EXP_44188_4#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489638</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G10, constructed from sample accession ERS9756445 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTGCAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109610</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489639" alias="SC_EXP_44188_4#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489639</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H10, constructed from sample accession ERS9756447 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TGCGGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756447">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="524" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489640" alias="SC_EXP_44188_4#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489640</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A11, constructed from sample accession ERS9756448 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence AAATGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756448">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="528" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489641" alias="SC_EXP_44188_4#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489641</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B11, constructed from sample accession ERS9756449 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TCACAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756449">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109614</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="523" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489642" alias="SC_EXP_44188_4#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489642</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C11, constructed from sample accession ERS9756450 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence AATGCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109615</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="513" NOMINAL_SDEV="161"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489643" alias="SC_EXP_44188_4#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489643</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D11, constructed from sample accession ERS9756451 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CGATAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489644" alias="SC_EXP_44188_4#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489644</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E11, constructed from sample accession ERS9756453 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GAGCATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756453">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109618</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="67"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489645" alias="SC_EXP_44188_4#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489645</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F11, constructed from sample accession ERS9756452 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTCTTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109617</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489646" alias="SC_EXP_44188_4#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489646</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G11, constructed from sample accession ERS9756454 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGGCCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756454">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489647" alias="SC_EXP_44188_4#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489647</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:H11, constructed from sample accession ERS9756455 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CACCTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109619</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="524" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489648" alias="SC_EXP_44188_4#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489648</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:A12, constructed from sample accession ERS9756456 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CCGATCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109621</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="524" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489649" alias="SC_EXP_44188_4#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489649</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:B12, constructed from sample accession ERS9756457 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GGCGTCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109622</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="63"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489650" alias="SC_EXP_44188_4#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489650</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:C12, constructed from sample accession ERS9756458 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GTCGGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109624</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="516" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489651" alias="SC_EXP_44188_4#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489651</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:D12, constructed from sample accession ERS9756459 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CTATACCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756459">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="505" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489652" alias="SC_EXP_44188_4#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489652</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:E12, constructed from sample accession ERS9756460 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence TTAAACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756460">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489653" alias="SC_EXP_44188_4#94" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489653</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:F12, constructed from sample accession ERS9756462 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence CACTCTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756462">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="546" NOMINAL_SDEV="140"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489654" alias="SC_EXP_44188_4#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489654</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_4#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882261F:G12, constructed from sample accession ERS9756463 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_4).  This submission includes reads tagged with the sequence GCAGCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9756463">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9756463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12109628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882261F:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="523" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489655" alias="SC_EXP_44188_5#1" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489655</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A1, constructed from sample accession ERS10430517 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CCGTTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430517">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823580</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="583" NOMINAL_SDEV="157"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489656" alias="SC_EXP_44188_5#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489656</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B1, constructed from sample accession ERS10430520 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TCGACTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430520">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430520</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823583</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="547" NOMINAL_SDEV="164"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489657" alias="SC_EXP_44188_5#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489657</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C1, constructed from sample accession ERS10430833 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGTAAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430833">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430833</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823719</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="573" NOMINAL_SDEV="153"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489658" alias="SC_EXP_44188_5#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489658</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D1, constructed from sample accession ERS10430836 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGTCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430836">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823730</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="60"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489659" alias="SC_EXP_44188_5#5" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489659</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E1, constructed from sample accession ERS10430837 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTCTCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430837">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430837</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="573" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489660" alias="SC_EXP_44188_5#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489660</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F1, constructed from sample accession ERS10430838 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TCTCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430838">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="31"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489661" alias="SC_EXP_44188_5#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489661</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G1, constructed from sample accession ERS10430841 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TCGGGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430841">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="541" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489662" alias="SC_EXP_44188_5#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489662</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H1, constructed from sample accession ERS10430845 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGAACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="588" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489663" alias="SC_EXP_44188_5#9" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489663</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A2, constructed from sample accession ERS10430849 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TGTTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430849">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430849</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="559" NOMINAL_SDEV="166"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489664" alias="SC_EXP_44188_5#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489664</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B2, constructed from sample accession ERS10430858 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TCCACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430858">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="561" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489665" alias="SC_EXP_44188_5#11" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489665</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C2, constructed from sample accession ERS10430857 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGCCTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489666" alias="SC_EXP_44188_5#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489666</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D2, constructed from sample accession ERS10430864 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTCGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430864">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="548" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489667" alias="SC_EXP_44188_5#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489667</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E2, constructed from sample accession ERS10430865 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AGACGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430865">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430865</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="564" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489668" alias="SC_EXP_44188_5#14" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489668</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F2, constructed from sample accession ERS10430868 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AGTGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430868">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="563" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489669" alias="SC_EXP_44188_5#15" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489669</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G2, constructed from sample accession ERS10430869 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTTCAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430869">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="569" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489670" alias="SC_EXP_44188_5#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489670</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H2, constructed from sample accession ERS10430870 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CACTCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="569" NOMINAL_SDEV="154"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489671" alias="SC_EXP_44188_5#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489671</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A3, constructed from sample accession ERS10430873 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CCATGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430873">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="559" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489672" alias="SC_EXP_44188_5#18" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489672</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B3, constructed from sample accession ERS10430875 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCTTGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430875">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="513" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489673" alias="SC_EXP_44188_5#19" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489673</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C3, constructed from sample accession ERS10430880 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGGCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430880">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="562" NOMINAL_SDEV="149"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489674" alias="SC_EXP_44188_5#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489674</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D3, constructed from sample accession ERS10430512 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGTTCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823575</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489675" alias="SC_EXP_44188_5#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489675</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E3, constructed from sample accession ERS10430513 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTATATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430513">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823577</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="559" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489676" alias="SC_EXP_44188_5#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489676</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F3, constructed from sample accession ERS10430514 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCTAAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430514">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823576</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="554" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489677" alias="SC_EXP_44188_5#23" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489677</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G3, constructed from sample accession ERS10430515 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCGCCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430515">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430515</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823578</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="535" NOMINAL_SDEV="161"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489678" alias="SC_EXP_44188_5#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489678</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H3, constructed from sample accession ERS10430516 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGCTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430516">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430516</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823579</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="584" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489679" alias="SC_EXP_44188_5#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489679</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A4, constructed from sample accession ERS10430519 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CACCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430519">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823582</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="563" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489680" alias="SC_EXP_44188_5#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489680</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B4, constructed from sample accession ERS10430518 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGCTGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430518">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823581</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="557" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489681" alias="SC_EXP_44188_5#27" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489681</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C4, constructed from sample accession ERS10430521 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence ACGTTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430521">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430521</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823584</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="555" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489682" alias="SC_EXP_44188_5#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489682</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D4, constructed from sample accession ERS10430522 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGCTTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430522">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430522</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="54"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489683" alias="SC_EXP_44188_5#29" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489683</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E4, constructed from sample accession ERS10430523 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGACGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430523">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430523</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823586</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="574" NOMINAL_SDEV="147"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489684" alias="SC_EXP_44188_5#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489684</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F4, constructed from sample accession ERS10430524 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GTGCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430524">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430524</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823587</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="539" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489685" alias="SC_EXP_44188_5#31" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489685</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G4, constructed from sample accession ERS10430525 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AGCATCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430525">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430525</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="151"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489686" alias="SC_EXP_44188_5#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489686</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H4, constructed from sample accession ERS10430526 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CACGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430526">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430526</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="541" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489687" alias="SC_EXP_44188_5#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489687</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A5, constructed from sample accession ERS10430527 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGAGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430527">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430527</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="511" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489688" alias="SC_EXP_44188_5#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489688</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B5, constructed from sample accession ERS10430528 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGGTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430528">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430528</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489689" alias="SC_EXP_44188_5#35" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489689</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C5, constructed from sample accession ERS10430531 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTAATCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430531">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430531</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489690" alias="SC_EXP_44188_5#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489690</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D5, constructed from sample accession ERS10430530 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTTATGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430530">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430530</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="575" NOMINAL_SDEV="148"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489691" alias="SC_EXP_44188_5#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489691</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E5, constructed from sample accession ERS10430529 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GTATGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430529">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430529</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823593</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="530" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489692" alias="SC_EXP_44188_5#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489692</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F5, constructed from sample accession ERS10430532 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTGTTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430532">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430532</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="579" NOMINAL_SDEV="154"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489693" alias="SC_EXP_44188_5#39" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489693</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G5, constructed from sample accession ERS10430533 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TATATTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430533">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430533</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="544" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489694" alias="SC_EXP_44188_5#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489694</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H5, constructed from sample accession ERS10430535 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AGACCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430535">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430535</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="591" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489695" alias="SC_EXP_44188_5#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489695</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A6, constructed from sample accession ERS10430534 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430534">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430534</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="564" NOMINAL_SDEV="152"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489696" alias="SC_EXP_44188_5#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489696</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B6, constructed from sample accession ERS10430640 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTTGGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430640">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430640</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="526" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489697" alias="SC_EXP_44188_5#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489697</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C6, constructed from sample accession ERS10430659 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CCGAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430659">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430659</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="516" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489698" alias="SC_EXP_44188_5#44" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489698</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D6, constructed from sample accession ERS10430747 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGTCGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430747">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430747</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="541" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489699" alias="SC_EXP_44188_5#45" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489699</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E6, constructed from sample accession ERS10430750 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence ATCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430750">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430750</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="541" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489700" alias="SC_EXP_44188_5#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489700</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F6, constructed from sample accession ERS10430753 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TGGGCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430753">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430753</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823606</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="547" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489701" alias="SC_EXP_44188_5#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489701</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G6, constructed from sample accession ERS10430814 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGGCACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="563" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489702" alias="SC_EXP_44188_5#48" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489702</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H6, constructed from sample accession ERS10430815 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CAAATAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430815">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430815</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823622</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="542" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489703" alias="SC_EXP_44188_5#49" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489703</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A7, constructed from sample accession ERS10430816 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CCTTCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430816">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823619</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="564" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489704" alias="SC_EXP_44188_5#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489704</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B7, constructed from sample accession ERS10430817 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTTAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430817">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="546" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489705" alias="SC_EXP_44188_5#51" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489705</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C7, constructed from sample accession ERS10430818 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AATAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430818">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430818</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="549" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489706" alias="SC_EXP_44188_5#52" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489706</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D7, constructed from sample accession ERS10430821 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGTTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430821">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430821</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="558" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489707" alias="SC_EXP_44188_5#53" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489707</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E7, constructed from sample accession ERS10430819 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCGTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430819">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="534" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489708" alias="SC_EXP_44188_5#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489708</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F7, constructed from sample accession ERS10430820 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGGACTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430820">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430820</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="576" NOMINAL_SDEV="147"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489709" alias="SC_EXP_44188_5#55" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489709</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G7, constructed from sample accession ERS10430822 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTGGGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430822">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430822</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="556" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489710" alias="SC_EXP_44188_5#56" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489710</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H7, constructed from sample accession ERS10430823 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GATATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430823">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430823</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="555" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489711" alias="SC_EXP_44188_5#57" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489711</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A8, constructed from sample accession ERS10430824 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AATGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430824">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430824</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="556" NOMINAL_SDEV="149"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489712" alias="SC_EXP_44188_5#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489712</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B8, constructed from sample accession ERS10430826 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCAATAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430826">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="527" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489713" alias="SC_EXP_44188_5#59" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489713</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C8, constructed from sample accession ERS10430825 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430825">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="548" NOMINAL_SDEV="127"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489714" alias="SC_EXP_44188_5#60" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489714</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D8, constructed from sample accession ERS10430830 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TCGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430830">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823712</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489715" alias="SC_EXP_44188_5#61" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489715</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E8, constructed from sample accession ERS10430827 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCCGCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430827">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430827</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="518" NOMINAL_SDEV="146"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489716" alias="SC_EXP_44188_5#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489716</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F8, constructed from sample accession ERS10430828 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCAAACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="560" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489717" alias="SC_EXP_44188_5#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489717</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G8, constructed from sample accession ERS10430829 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCCGATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430829">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430829</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="563" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489718" alias="SC_EXP_44188_5#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489718</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H8, constructed from sample accession ERS10430831 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CACGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="4"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489719" alias="SC_EXP_44188_5#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489719</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A9, constructed from sample accession ERS10430832 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430832">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823706</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489720" alias="SC_EXP_44188_5#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489720</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B9, constructed from sample accession ERS10430834 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TCTGAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430834">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823727</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="548" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489721" alias="SC_EXP_44188_5#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489721</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C9, constructed from sample accession ERS10430835 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGGAAAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430835">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430835</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823731</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="549" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489722" alias="SC_EXP_44188_5#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489722</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D9, constructed from sample accession ERS10430839 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTGGTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="570" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489723" alias="SC_EXP_44188_5#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489723</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E9, constructed from sample accession ERS10430840 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTTGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430840">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430840</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="538" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489724" alias="SC_EXP_44188_5#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489724</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F9, constructed from sample accession ERS10430843 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CCAGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430843">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="67"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489725" alias="SC_EXP_44188_5#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489725</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G9, constructed from sample accession ERS10430842 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GTGGGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="569" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489726" alias="SC_EXP_44188_5#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489726</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H9, constructed from sample accession ERS10430844 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGGACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430844">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430844</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="547" NOMINAL_SDEV="147"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489727" alias="SC_EXP_44188_5#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489727</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A10, constructed from sample accession ERS10430847 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GTTGACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430847">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430847</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="551" NOMINAL_SDEV="121"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489728" alias="SC_EXP_44188_5#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489728</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B10, constructed from sample accession ERS10430846 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGGGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430846">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430846</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="530" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489729" alias="SC_EXP_44188_5#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489729</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C10, constructed from sample accession ERS10430848 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GAGACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="564" NOMINAL_SDEV="140"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489730" alias="SC_EXP_44188_5#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489730</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D10, constructed from sample accession ERS10430850 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCCAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430850">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430850</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="23"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489731" alias="SC_EXP_44188_5#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489731</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E10, constructed from sample accession ERS10430851 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGCGTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="556" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489732" alias="SC_EXP_44188_5#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489732</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F10, constructed from sample accession ERS10430852 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGTAGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430852">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430852</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="568" NOMINAL_SDEV="140"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489733" alias="SC_EXP_44188_5#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489733</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G10, constructed from sample accession ERS10430854 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence ACGCGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="554" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489734" alias="SC_EXP_44188_5#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489734</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H10, constructed from sample accession ERS10430853 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GTGACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430853">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430853</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="562" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489735" alias="SC_EXP_44188_5#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489735</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A11, constructed from sample accession ERS10430855 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GTTTGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430855">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430855</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="546" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489736" alias="SC_EXP_44188_5#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489736</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B11, constructed from sample accession ERS10430856 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GCACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430856">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430856</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="558" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489737" alias="SC_EXP_44188_5#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489737</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C11, constructed from sample accession ERS10430859 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTTTAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430859">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="559" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489738" alias="SC_EXP_44188_5#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489738</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D11, constructed from sample accession ERS10430860 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TGTAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="557" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489739" alias="SC_EXP_44188_5#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489739</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E11, constructed from sample accession ERS10430861 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TTCACGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430861">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="556" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489740" alias="SC_EXP_44188_5#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489740</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F11, constructed from sample accession ERS10430862 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GATGAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430862">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="545" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489741" alias="SC_EXP_44188_5#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489741</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G11, constructed from sample accession ERS10430863 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGCGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="547" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489742" alias="SC_EXP_44188_5#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489742</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H11, constructed from sample accession ERS10430866 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AACCTGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="552" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489743" alias="SC_EXP_44188_5#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489743</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:A12, constructed from sample accession ERS10430867 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence GGTTAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430867">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="536" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489744" alias="SC_EXP_44188_5#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489744</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:B12, constructed from sample accession ERS10430871 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGGGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430871">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="520" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489745" alias="SC_EXP_44188_5#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489745</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:C12, constructed from sample accession ERS10430874 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTTGTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430874">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489746" alias="SC_EXP_44188_5#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489746</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:D12, constructed from sample accession ERS10430872 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence AAAGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430872">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="23"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489747" alias="SC_EXP_44188_5#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489747</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:E12, constructed from sample accession ERS10430876 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence TCAGTTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430876">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="551" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489748" alias="SC_EXP_44188_5#94" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489748</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:F12, constructed from sample accession ERS10430877 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CGGTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430877">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="498" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489749" alias="SC_EXP_44188_5#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489749</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:G12, constructed from sample accession ERS10430878 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CCAGCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430878">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="554" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX10489750" alias="SC_EXP_44188_5#96" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX10489750</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_44188_5#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP124013">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP124013</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB40384</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881205Q:H12, constructed from sample accession ERS10430879 for study accession ERP124013.  This is part of an Illumina multiplexed sequencing run (44188_5).  This submission includes reads tagged with the sequence CTGCCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS10430879">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS10430879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12823939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881205Q:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="532" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
