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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX9364982" alias="SC_EXP_21878_5#1" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364982</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A1, constructed from sample accession ERS1284243 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364983" alias="SC_EXP_21878_5#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364983</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B1, constructed from sample accession ERS1284244 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="487" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364984" alias="SC_EXP_21878_5#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364984</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C1, constructed from sample accession ERS1284245 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364985" alias="SC_EXP_21878_5#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364985</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D1, constructed from sample accession ERS1284246 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284246">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284246</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D1</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="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364986" alias="SC_EXP_21878_5#5" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364986</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E1, constructed from sample accession ERS1284247 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364987" alias="SC_EXP_21878_5#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364987</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F1, constructed from sample accession ERS1284248 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284248">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="496" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364988" alias="SC_EXP_21878_5#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364988</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G1, constructed from sample accession ERS1284249 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284249">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364989" alias="SC_EXP_21878_5#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364989</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H1, constructed from sample accession ERS1284250 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284250">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364990" alias="SC_EXP_21878_5#9" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364990</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A2, constructed from sample accession ERS1284251 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A2</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="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364991" alias="SC_EXP_21878_5#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364991</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B2, constructed from sample accession ERS1284252 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B2</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364992" alias="SC_EXP_21878_5#11" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364992</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C2, constructed from sample accession ERS1284253 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284253">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="496" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364993" alias="SC_EXP_21878_5#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364993</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D2, constructed from sample accession ERS1284254 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364994" alias="SC_EXP_21878_5#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364994</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E2, constructed from sample accession ERS1284255 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="499" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364995" alias="SC_EXP_21878_5#14" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364995</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F2, constructed from sample accession ERS1284256 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284256">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284256</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F2</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="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364996" alias="SC_EXP_21878_5#15" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364996</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G2, constructed from sample accession ERS1284257 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="490" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364997" alias="SC_EXP_21878_5#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364997</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H2, constructed from sample accession ERS1284258 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="501" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364998" alias="SC_EXP_21878_5#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364998</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A3, constructed from sample accession ERS1284259 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284259">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9364999" alias="SC_EXP_21878_5#18" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9364999</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B3, constructed from sample accession ERS1284260 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284260">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284260</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365000" alias="SC_EXP_21878_5#19" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365000</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C3, constructed from sample accession ERS1284261 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F: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="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365001" alias="SC_EXP_21878_5#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365001</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D3, constructed from sample accession ERS1284262 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284262">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284262</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365002" alias="SC_EXP_21878_5#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365002</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E3, constructed from sample accession ERS1284263 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E3</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="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365003" alias="SC_EXP_21878_5#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365003</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F3, constructed from sample accession ERS1284264 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="493" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365004" alias="SC_EXP_21878_5#23" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365004</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G3, constructed from sample accession ERS1284265 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284265">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284265</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G3</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="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365005" alias="SC_EXP_21878_5#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365005</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H3, constructed from sample accession ERS1284266 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H3</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="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365006" alias="SC_EXP_21878_5#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365006</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A4, constructed from sample accession ERS1284267 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284267">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284267</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365007" alias="SC_EXP_21878_5#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365007</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B4, constructed from sample accession ERS1284268 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284268">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284268</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365008" alias="SC_EXP_21878_5#27" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365008</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C4, constructed from sample accession ERS1284269 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365009" alias="SC_EXP_21878_5#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365009</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D4, constructed from sample accession ERS1284270 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="490" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365010" alias="SC_EXP_21878_5#29" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365010</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E4, constructed from sample accession ERS1284271 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284271">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365011" alias="SC_EXP_21878_5#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365011</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F4, constructed from sample accession ERS1284272 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F4</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="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365012" alias="SC_EXP_21878_5#31" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365012</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G4, constructed from sample accession ERS1284273 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365013" alias="SC_EXP_21878_5#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365013</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H4, constructed from sample accession ERS1284274 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H4</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="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365014" alias="SC_EXP_21878_5#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365014</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A5, constructed from sample accession ERS1284275 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365015" alias="SC_EXP_21878_5#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365015</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B5, constructed from sample accession ERS1284276 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365016" alias="SC_EXP_21878_5#35" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365016</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C5, constructed from sample accession ERS1284277 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="488" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365017" alias="SC_EXP_21878_5#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365017</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D5, constructed from sample accession ERS1284278 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365018" alias="SC_EXP_21878_5#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365018</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E5, constructed from sample accession ERS1284279 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E5</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="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365019" alias="SC_EXP_21878_5#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365019</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F5, constructed from sample accession ERS1284280 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F5</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="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365020" alias="SC_EXP_21878_5#39" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365020</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G5, constructed from sample accession ERS1284281 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="509" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365021" alias="SC_EXP_21878_5#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365021</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H5, constructed from sample accession ERS1284282 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284282">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365022" alias="SC_EXP_21878_5#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365022</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A6, constructed from sample accession ERS1284283 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284283">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365023" alias="SC_EXP_21878_5#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365023</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B6, constructed from sample accession ERS1284284 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B6</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="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365024" alias="SC_EXP_21878_5#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365024</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C6, constructed from sample accession ERS1284285 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284285">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="503" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365025" alias="SC_EXP_21878_5#44" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365025</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D6, constructed from sample accession ERS1284286 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284286">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284286</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D6</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="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365026" alias="SC_EXP_21878_5#45" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365026</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E6, constructed from sample accession ERS1284287 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284287">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284287</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365027" alias="SC_EXP_21878_5#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365027</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F6, constructed from sample accession ERS1284288 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284288">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365028" alias="SC_EXP_21878_5#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365028</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G6, constructed from sample accession ERS1284289 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365029" alias="SC_EXP_21878_5#48" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365029</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H6, constructed from sample accession ERS1284290 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365030" alias="SC_EXP_21878_5#49" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365030</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A7, constructed from sample accession ERS1284291 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284291">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365031" alias="SC_EXP_21878_5#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365031</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B7, constructed from sample accession ERS1284292 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="489" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365032" alias="SC_EXP_21878_5#51" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365032</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C7, constructed from sample accession ERS1284293 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365033" alias="SC_EXP_21878_5#52" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365033</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D7, constructed from sample accession ERS1284294 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="496" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365034" alias="SC_EXP_21878_5#53" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365034</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E7, constructed from sample accession ERS1284295 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365035" alias="SC_EXP_21878_5#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365035</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F7, constructed from sample accession ERS1284296 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365036" alias="SC_EXP_21878_5#55" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365036</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G7, constructed from sample accession ERS1284297 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284297">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365037" alias="SC_EXP_21878_5#56" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365037</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H7, constructed from sample accession ERS1284298 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H7</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="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365038" alias="SC_EXP_21878_5#57" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365038</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A8, constructed from sample accession ERS1284299 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365039" alias="SC_EXP_21878_5#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365039</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B8, constructed from sample accession ERS1284300 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B8</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="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365040" alias="SC_EXP_21878_5#59" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365040</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C8, constructed from sample accession ERS1284301 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C8</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="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365041" alias="SC_EXP_21878_5#60" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365041</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D8, constructed from sample accession ERS1284302 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365042" alias="SC_EXP_21878_5#61" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365042</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E8, constructed from sample accession ERS1284303 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365043" alias="SC_EXP_21878_5#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365043</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F8, constructed from sample accession ERS1284304 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365044" alias="SC_EXP_21878_5#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365044</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G8, constructed from sample accession ERS1284305 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G8</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="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365045" alias="SC_EXP_21878_5#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365045</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H8, constructed from sample accession ERS1284306 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H8</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="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365046" alias="SC_EXP_21878_5#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365046</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A9, constructed from sample accession ERS1284307 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365047" alias="SC_EXP_21878_5#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365047</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B9, constructed from sample accession ERS1284308 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365048" alias="SC_EXP_21878_5#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365048</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C9, constructed from sample accession ERS1284309 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="487" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365049" alias="SC_EXP_21878_5#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365049</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D9, constructed from sample accession ERS1284310 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365050" alias="SC_EXP_21878_5#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365050</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E9, constructed from sample accession ERS1284311 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365051" alias="SC_EXP_21878_5#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365051</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F9, constructed from sample accession ERS1284312 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365052" alias="SC_EXP_21878_5#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365052</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G9, constructed from sample accession ERS1284313 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G9</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="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365053" alias="SC_EXP_21878_5#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365053</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H9, constructed from sample accession ERS1284314 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H9</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="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365054" alias="SC_EXP_21878_5#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365054</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A10, constructed from sample accession ERS1284315 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365055" alias="SC_EXP_21878_5#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365055</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B10, constructed from sample accession ERS1284316 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365056" alias="SC_EXP_21878_5#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365056</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C10, constructed from sample accession ERS1284317 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284317">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365057" alias="SC_EXP_21878_5#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365057</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D10, constructed from sample accession ERS1284318 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365058" alias="SC_EXP_21878_5#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365058</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E10, constructed from sample accession ERS1284319 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365059" alias="SC_EXP_21878_5#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365059</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F10, constructed from sample accession ERS1284320 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365060" alias="SC_EXP_21878_5#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365060</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G10, constructed from sample accession ERS1284321 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365061" alias="SC_EXP_21878_5#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365061</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H10, constructed from sample accession ERS1284322 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365062" alias="SC_EXP_21878_5#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365062</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A11, constructed from sample accession ERS1284323 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365063" alias="SC_EXP_21878_5#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365063</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B11, constructed from sample accession ERS1284324 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B11</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="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365064" alias="SC_EXP_21878_5#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365064</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C11, constructed from sample accession ERS1284325 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365065" alias="SC_EXP_21878_5#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365065</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D11, constructed from sample accession ERS1284326 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D11</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="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365066" alias="SC_EXP_21878_5#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365066</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E11, constructed from sample accession ERS1284327 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284327">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365067" alias="SC_EXP_21878_5#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365067</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F11, constructed from sample accession ERS1284328 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365068" alias="SC_EXP_21878_5#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365068</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G11, constructed from sample accession ERS1284329 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365069" alias="SC_EXP_21878_5#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365069</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H11, constructed from sample accession ERS1284330 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GATAGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365070" alias="SC_EXP_21878_5#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365070</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:A12, constructed from sample accession ERS1284331 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365071" alias="SC_EXP_21878_5#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365071</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:B12, constructed from sample accession ERS1284332 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365072" alias="SC_EXP_21878_5#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365072</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:C12, constructed from sample accession ERS1284333 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365073" alias="SC_EXP_21878_5#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365073</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:D12, constructed from sample accession ERS1284334 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365074" alias="SC_EXP_21878_5#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365074</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:E12, constructed from sample accession ERS1284335 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="487" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365075" alias="SC_EXP_21878_5#94" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365075</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:F12, constructed from sample accession ERS1284336 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365076" alias="SC_EXP_21878_5#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365076</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:G12, constructed from sample accession ERS1284337 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365077" alias="SC_EXP_21878_5#96" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365077</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21878_5#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN469178F:H12, constructed from sample accession ERS1284338 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (21878_5).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1284338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1284338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA4372889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN469178F:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365078" alias="SC_EXP_25858_1#1" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365078</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:A1, constructed from sample accession ERS12125628 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125628">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125628</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:A1</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365079" alias="SC_EXP_25858_1#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365079</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:B1, constructed from sample accession ERS12125629 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125629">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125629</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365080" alias="SC_EXP_25858_1#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365080</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:C1, constructed from sample accession ERS12125630 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125630">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125630</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110031708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365081" alias="SC_EXP_25858_1#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365081</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:D1, constructed from sample accession ERS12125631 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125631">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125631</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110031709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:D1</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="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365082" alias="SC_EXP_25858_1#5" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365082</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:E1, constructed from sample accession ERS12125632 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125632">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495514</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365083" alias="SC_EXP_25858_1#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365083</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:F1, constructed from sample accession ERS12125633 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125633">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110043658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365084" alias="SC_EXP_25858_1#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365084</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:G1, constructed from sample accession ERS12125636 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125636">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495516</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365085" alias="SC_EXP_25858_1#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365085</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:H1, constructed from sample accession ERS12125634 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125634">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:H1</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="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365086" alias="SC_EXP_25858_1#9" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365086</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:A2, constructed from sample accession ERS12125635 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125635">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125635</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110037283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365087" alias="SC_EXP_25858_1#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365087</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:B2, constructed from sample accession ERS12125637 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125637">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495517</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365088" alias="SC_EXP_25858_1#11" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365088</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:C2, constructed from sample accession ERS12125639 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125639">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125639</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110031710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365089" alias="SC_EXP_25858_1#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365089</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:D2, constructed from sample accession ERS12125638 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125638">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125638</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365090" alias="SC_EXP_25858_1#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365090</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:E2, constructed from sample accession ERS12125640 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125640">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125640</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:E2</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="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365091" alias="SC_EXP_25858_1#14" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365091</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:F2, constructed from sample accession ERS12125641 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125641">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125641</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:F2</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="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365092" alias="SC_EXP_25858_1#15" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365092</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:G2, constructed from sample accession ERS12125642 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125642">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125642</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110054756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:G2</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="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365093" alias="SC_EXP_25858_1#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365093</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:H2, constructed from sample accession ERS12125643 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125643">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125643</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110054757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365094" alias="SC_EXP_25858_1#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365094</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:A3, constructed from sample accession ERS12125645 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125645">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125645</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365095" alias="SC_EXP_25858_1#18" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365095</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:B3, constructed from sample accession ERS12125644 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125644">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125644</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365096" alias="SC_EXP_25858_1#19" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365096</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:C3, constructed from sample accession ERS12125646 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125646">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:C3</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365097" alias="SC_EXP_25858_1#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365097</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:D3, constructed from sample accession ERS12125647 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125647">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:D3</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="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365098" alias="SC_EXP_25858_1#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365098</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:E3, constructed from sample accession ERS12125649 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125649">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365099" alias="SC_EXP_25858_1#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365099</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:F3, constructed from sample accession ERS12125648 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125648">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110049258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365100" alias="SC_EXP_25858_1#23" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365100</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:G3, constructed from sample accession ERS12125650 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125650">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125650</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365101" alias="SC_EXP_25858_1#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365101</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:H3, constructed from sample accession ERS12125651 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125651">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110026965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365102" alias="SC_EXP_25858_1#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365102</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:A4, constructed from sample accession ERS12125652 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125652">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110043659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:A4</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365103" alias="SC_EXP_25858_1#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365103</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:B4, constructed from sample accession ERS12125653 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125653">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365104" alias="SC_EXP_25858_1#27" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365104</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:C4, constructed from sample accession ERS12125654 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125654">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125654</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110049259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365105" alias="SC_EXP_25858_1#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365105</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:D4, constructed from sample accession ERS12125655 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125655">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125655</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:D4</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365106" alias="SC_EXP_25858_1#29" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365106</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:E4, constructed from sample accession ERS12125656 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125656">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125656</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:E4</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="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365107" alias="SC_EXP_25858_1#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365107</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:F4, constructed from sample accession ERS12125657 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125657">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125657</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110031711</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:F4</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365108" alias="SC_EXP_25858_1#31" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365108</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:G4, constructed from sample accession ERS12125658 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125658">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125658</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110054758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:G4</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365109" alias="SC_EXP_25858_1#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365109</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:H4, constructed from sample accession ERS12125659 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125659">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125659</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:H4</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="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365110" alias="SC_EXP_25858_1#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365110</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:A5, constructed from sample accession ERS12125661 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125661">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125661</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495531</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365111" alias="SC_EXP_25858_1#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365111</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:B5, constructed from sample accession ERS12125660 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125660">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125660</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110054759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:B5</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="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365112" alias="SC_EXP_25858_1#35" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365112</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:C5, constructed from sample accession ERS12125662 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125662">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125662</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:C5</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="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365113" alias="SC_EXP_25858_1#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365113</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:D5, constructed from sample accession ERS12125663 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125663">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125663</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110017991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365114" alias="SC_EXP_25858_1#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365114</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:E5, constructed from sample accession ERS12125664 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125664">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125664</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="459" NOMINAL_SDEV="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365115" alias="SC_EXP_25858_1#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365115</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:F5, constructed from sample accession ERS12125665 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125665">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125665</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110017993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:F5</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="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365116" alias="SC_EXP_25858_1#39" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365116</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:G5, constructed from sample accession ERS12125666 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125666">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125666</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110054760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:G5</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="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365117" alias="SC_EXP_25858_1#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365117</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:H5, constructed from sample accession ERS12125667 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125667">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125667</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:H5</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="118"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365118" alias="SC_EXP_25858_1#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365118</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:A6, constructed from sample accession ERS12125668 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125668">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125668</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110017990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365119" alias="SC_EXP_25858_1#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365119</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:B6, constructed from sample accession ERS12125669 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125669">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125669</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365120" alias="SC_EXP_25858_1#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365120</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:C6, constructed from sample accession ERS12125670 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125670">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125670</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365121" alias="SC_EXP_25858_1#44" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365121</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:D6, constructed from sample accession ERS12125671 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125671">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125671</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110017992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:D6</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="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365122" alias="SC_EXP_25858_1#45" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365122</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:E6, constructed from sample accession ERS12125672 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125672">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125672</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110049260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365123" alias="SC_EXP_25858_1#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365123</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:F6, constructed from sample accession ERS12125673 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125673">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125673</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA14495537</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365124" alias="SC_EXP_25858_1#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365124</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:G6, constructed from sample accession ERS12125674 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125674">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125674</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110049261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:G6</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX9365125" alias="SC_EXP_25858_1#48" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX9365125</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_25858_1#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP011749">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP011749</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB10486</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN514214W:H6, constructed from sample accession ERS12125675 for study accession ERP011749.  This is part of an Illumina multiplexed sequencing run (25858_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS12125675">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS12125675</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA110049262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN514214W:H6</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="121"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
