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  <EXPERIMENT accession="ERX4442526" alias="SC_EXP_30564_5#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:A1, constructed from sample accession ERS3498442 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442527" alias="SC_EXP_30564_5#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:B1, constructed from sample accession ERS3498443 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498443">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442528" alias="SC_EXP_30564_5#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:C1, constructed from sample accession ERS3498444 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498444">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442529" alias="SC_EXP_30564_5#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:D1, constructed from sample accession ERS3498445 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GATCAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442530" alias="SC_EXP_30564_5#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:E1, constructed from sample accession ERS3498446 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGAAGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498446">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442531" alias="SC_EXP_30564_5#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:F1, constructed from sample accession ERS3498450 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GATGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442532" alias="SC_EXP_30564_5#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:G1, constructed from sample accession ERS3498451 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTACGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442533" alias="SC_EXP_30564_5#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:H1, constructed from sample accession ERS3498452 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GATGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442534" alias="SC_EXP_30564_5#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:A2, constructed from sample accession ERS3498453 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498453">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694493</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442535" alias="SC_EXP_30564_5#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:B2, constructed from sample accession ERS3498454 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498454">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442536" alias="SC_EXP_30564_5#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:C2, constructed from sample accession ERS3498455 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTACTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442537" alias="SC_EXP_30564_5#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:D2, constructed from sample accession ERS3498456 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442538" alias="SC_EXP_30564_5#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:E2, constructed from sample accession ERS3498457 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence AATCGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442539" alias="SC_EXP_30564_5#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:F2, constructed from sample accession ERS3498458 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TTCGCCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694498</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442540" alias="SC_EXP_30564_5#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:G2, constructed from sample accession ERS3498459 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTGGCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498459">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442541" alias="SC_EXP_30564_5#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:H2, constructed from sample accession ERS3498460 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498460">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442542" alias="SC_EXP_30564_5#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:A3, constructed from sample accession ERS3498461 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGTATTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498461">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498461</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442543" alias="SC_EXP_30564_5#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:B3, constructed from sample accession ERS3498462 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498462">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442544" alias="SC_EXP_30564_5#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:C3, constructed from sample accession ERS3498463 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498463">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442545" alias="SC_EXP_30564_5#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:D3, constructed from sample accession ERS3498464 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498464">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442546" alias="SC_EXP_30564_5#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:E3, constructed from sample accession ERS3498465 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAAGAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498465">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442547" alias="SC_EXP_30564_5#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:F3, constructed from sample accession ERS3498466 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498466">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694506</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442548" alias="SC_EXP_30564_5#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:G3, constructed from sample accession ERS3498467 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAATCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498467">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442549" alias="SC_EXP_30564_5#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:H3, constructed from sample accession ERS3498468 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498468">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442550" alias="SC_EXP_30564_5#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:A4, constructed from sample accession ERS3498469 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence AATCCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498469">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442551" alias="SC_EXP_30564_5#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:B4, constructed from sample accession ERS3498471 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TGCGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498471">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498471</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694511</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442552" alias="SC_EXP_30564_5#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:C4, constructed from sample accession ERS3498472 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498472">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442553" alias="SC_EXP_30564_5#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:D4, constructed from sample accession ERS3498473 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TGAGTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498473">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442554" alias="SC_EXP_30564_5#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:E4, constructed from sample accession ERS3498474 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAATGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498474">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694514</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442555" alias="SC_EXP_30564_5#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:F4, constructed from sample accession ERS3498475 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GAATATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498475">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498475</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442556" alias="SC_EXP_30564_5#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:G4, constructed from sample accession ERS3498476 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498476">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498476</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694516</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442557" alias="SC_EXP_30564_5#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:H4, constructed from sample accession ERS3498477 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TCGGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498477">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498477</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694517</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442558" alias="SC_EXP_30564_5#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:A5, constructed from sample accession ERS3498478 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence AAGAAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442559" alias="SC_EXP_30564_5#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:B5, constructed from sample accession ERS3498479 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498479">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498479</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442560" alias="SC_EXP_30564_5#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:C5, constructed from sample accession ERS3498480 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TCGGTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498480">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498480</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442561" alias="SC_EXP_30564_5#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:D5, constructed from sample accession ERS3498481 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498481">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498481</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442562" alias="SC_EXP_30564_5#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:E5, constructed from sample accession ERS3498482 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498482">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498482</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442563" alias="SC_EXP_30564_5#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:F5, constructed from sample accession ERS3498483 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498483">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498483</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442564" alias="SC_EXP_30564_5#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:G5, constructed from sample accession ERS3498484 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TCGGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498484">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498484</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442565" alias="SC_EXP_30564_5#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:H5, constructed from sample accession ERS3498485 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGAGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498485">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498485</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442566" alias="SC_EXP_30564_5#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:A6, constructed from sample accession ERS3498486 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498486">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498486</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442567" alias="SC_EXP_30564_5#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:B6, constructed from sample accession ERS3498487 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence TCGAAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498487">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498487</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442568" alias="SC_EXP_30564_5#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:C6, constructed from sample accession ERS3498488 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498488">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498488</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442569" alias="SC_EXP_30564_5#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:D6, constructed from sample accession ERS3498489 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGCGCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498489">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498489</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442570" alias="SC_EXP_30564_5#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30564_5#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30564_5#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547401E:E6, constructed from sample accession ERS3498490 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30564_5).  This submission includes reads tagged with the sequence CGAACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498490">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498490</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547401E:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442571" alias="SC_EXP_30602_7#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A1, constructed from sample accession ERS3498382 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCGTTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:A1</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="130"/>
        </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="ERX4442572" alias="SC_EXP_30602_7#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A1, constructed from sample accession ERS3498279 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGGAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694318</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K: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="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="ERX4442573" alias="SC_EXP_30602_7#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B1, constructed from sample accession ERS3498383 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCGACTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B1</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="124"/>
        </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="ERX4442574" alias="SC_EXP_30602_7#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C1, constructed from sample accession ERS3498389 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGTAAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C1</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="125"/>
        </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="ERX4442575" alias="SC_EXP_30602_7#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D1, constructed from sample accession ERS3498390 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGTCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D1</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="122"/>
        </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="ERX4442576" alias="SC_EXP_30602_7#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E1, constructed from sample accession ERS3498392 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTCTCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498392">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E1</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="133"/>
        </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="ERX4442577" alias="SC_EXP_30602_7#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F1, constructed from sample accession ERS3498284 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TATTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F1</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="136"/>
        </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="ERX4442578" alias="SC_EXP_30602_7#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F1, constructed from sample accession ERS3498393 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCTCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F1</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="128"/>
        </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="ERX4442579" alias="SC_EXP_30602_7#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G1, constructed from sample accession ERS3498394 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCGGGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G1</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="129"/>
        </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="ERX4442580" alias="SC_EXP_30602_7#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G1, constructed from sample accession ERS3498285 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTACGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498285">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694324</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G1</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="122"/>
        </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="ERX4442581" alias="SC_EXP_30602_7#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H1, constructed from sample accession ERS3498395 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGAACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H1</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="120"/>
        </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="ERX4442582" alias="SC_EXP_30602_7#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H1, constructed from sample accession ERS3498286 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTGATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498286">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498286</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694325</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H1</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="129"/>
        </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="ERX4442583" alias="SC_EXP_30602_7#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A2, constructed from sample accession ERS3498287 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TATATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498287">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498287</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A2</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="123"/>
        </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="ERX4442584" alias="SC_EXP_30602_7#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A2, constructed from sample accession ERS3498396 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TGTTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:A2</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="126"/>
        </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="ERX4442585" alias="SC_EXP_30602_7#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B2, constructed from sample accession ERS3498397 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCCACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B2</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="129"/>
        </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="ERX4442586" alias="SC_EXP_30602_7#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B2, constructed from sample accession ERS3498288 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTATCCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498288">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694327</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B2</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="124"/>
        </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="ERX4442587" alias="SC_EXP_30602_7#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C2, constructed from sample accession ERS3498289 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTACCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694328</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C2</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="130"/>
        </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="ERX4442588" alias="SC_EXP_30602_7#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C2, constructed from sample accession ERS3498398 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGCCTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C2</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="123"/>
        </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="ERX4442589" alias="SC_EXP_30602_7#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D2, constructed from sample accession ERS3498400 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTCGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D2</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="128"/>
        </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="ERX4442590" alias="SC_EXP_30602_7#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D2, constructed from sample accession ERS3498290 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CAGAGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498290">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D2</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="131"/>
        </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="ERX4442591" alias="SC_EXP_30602_7#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E2, constructed from sample accession ERS3498401 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGACGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694441</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E2</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="122"/>
        </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="ERX4442592" alias="SC_EXP_30602_7#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F2, constructed from sample accession ERS3498292 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTTCCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F2</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="125"/>
        </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="ERX4442593" alias="SC_EXP_30602_7#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F2, constructed from sample accession ERS3498403 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGTGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F2</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="125"/>
        </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="ERX4442594" alias="SC_EXP_30602_7#54">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G2, constructed from sample accession ERS3498293 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TAGGCGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498293">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G2</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="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 accession="ERX4442595" alias="SC_EXP_30602_7#55">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G2, constructed from sample accession ERS3498404 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTTCAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="126"/>
        </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="ERX4442596" alias="SC_EXP_30602_7#58">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H2, constructed from sample accession ERS3498294 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GACTTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H2</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="130"/>
        </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="ERX4442597" alias="SC_EXP_30602_7#59">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H2, constructed from sample accession ERS3498405 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CACTCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498405">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694445</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H2</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="127"/>
        </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="ERX4442598" alias="SC_EXP_30602_7#62">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A3, constructed from sample accession ERS3498295 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCATCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A3</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="123"/>
        </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="ERX4442599" alias="SC_EXP_30602_7#63">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A3, constructed from sample accession ERS3498406 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCATGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498406">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694446</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L: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="123"/>
        </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="ERX4442600" alias="SC_EXP_30602_7#66">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B3, constructed from sample accession ERS3498296 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence ACTTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B3</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="136"/>
        </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="ERX4442601" alias="SC_EXP_30602_7#67">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B3, constructed from sample accession ERS3498407 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCTTGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498407">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B3</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="122"/>
        </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="ERX4442602" alias="SC_EXP_30602_7#70">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C3, constructed from sample accession ERS3498297 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCTAAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498297">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694336</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="486" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442603" alias="SC_EXP_30602_7#71">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C3, constructed from sample accession ERS3498408 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGGCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C3</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="128"/>
        </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="ERX4442604" alias="SC_EXP_30602_7#74">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D3, constructed from sample accession ERS3498298 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694337</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D3</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="153"/>
        </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="ERX4442605" alias="SC_EXP_30602_7#75">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D3, constructed from sample accession ERS3498409 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGTTCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D3</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="130"/>
        </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="ERX4442606" alias="SC_EXP_30602_7#78">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E3, constructed from sample accession ERS3498299 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTCCGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694338</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E3</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="128"/>
        </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="ERX4442607" alias="SC_EXP_30602_7#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E3, constructed from sample accession ERS3498410 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTATATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694450</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E3</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="122"/>
        </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="ERX4442608" alias="SC_EXP_30602_7#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F3, constructed from sample accession ERS3498300 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCGCTAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F3</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="128"/>
        </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="ERX4442609" alias="SC_EXP_30602_7#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F3, constructed from sample accession ERS3498411 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCTAAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F3</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="123"/>
        </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="ERX4442610" alias="SC_EXP_30602_7#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G3, constructed from sample accession ERS3498301 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCCACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G3</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="132"/>
        </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="ERX4442611" alias="SC_EXP_30602_7#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G3, constructed from sample accession ERS3498412 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCGCCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G3</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="128"/>
        </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="ERX4442612" alias="SC_EXP_30602_7#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H3, constructed from sample accession ERS3498302 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AACTTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498302">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694341</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H3</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="127"/>
        </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="ERX4442613" alias="SC_EXP_30602_7#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H3, constructed from sample accession ERS3498413 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGCTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H3</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="120"/>
        </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="ERX4442614" alias="SC_EXP_30602_7#94">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A4, constructed from sample accession ERS3498303 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTAACTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498303">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694342</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A4</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="131"/>
        </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="ERX4442615" alias="SC_EXP_30602_7#95">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A4, constructed from sample accession ERS3498414 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CACCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:A4</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="125"/>
        </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="ERX4442616" alias="SC_EXP_30602_7#98">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B4, constructed from sample accession ERS3498304 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTTGCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B4</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="128"/>
        </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="ERX4442617" alias="SC_EXP_30602_7#99">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B4, constructed from sample accession ERS3498415 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGCTGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B4</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="125"/>
        </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="ERX4442618" alias="SC_EXP_30602_7#102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C4, constructed from sample accession ERS3498305 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTTAGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C4</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="129"/>
        </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="ERX4442619" alias="SC_EXP_30602_7#103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C4, constructed from sample accession ERS3498416 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence ACGTTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C4</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="130"/>
        </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="ERX4442620" alias="SC_EXP_30602_7#106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D4, constructed from sample accession ERS3498306 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGTGGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498306">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694345</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D4</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="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="ERX4442621" alias="SC_EXP_30602_7#107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D4, constructed from sample accession ERS3498417 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGCTTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D4</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="135"/>
        </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="ERX4442622" alias="SC_EXP_30602_7#110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E4, constructed from sample accession ERS3498307 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence ATATGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694346</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E4</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="126"/>
        </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="ERX4442623" alias="SC_EXP_30602_7#111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E4, constructed from sample accession ERS3498418 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGACGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E4</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="133"/>
        </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="ERX4442624" alias="SC_EXP_30602_7#114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F4, constructed from sample accession ERS3498308 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498308">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694347</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F4</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="126"/>
        </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="ERX4442625" alias="SC_EXP_30602_7#115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F4, constructed from sample accession ERS3498419 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTGCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F4</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="125"/>
        </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="ERX4442626" alias="SC_EXP_30602_7#118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#118</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G4, constructed from sample accession ERS3498309 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGCCTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498309">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G4</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="141"/>
        </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="ERX4442627" alias="SC_EXP_30602_7#119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#119</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G4, constructed from sample accession ERS3498420 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGCATCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G4</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="128"/>
        </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="ERX4442628" alias="SC_EXP_30602_7#122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H4, constructed from sample accession ERS3498310 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGATAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H4</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="132"/>
        </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="ERX4442629" alias="SC_EXP_30602_7#123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H4, constructed from sample accession ERS3498421 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CACGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="123"/>
        </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="ERX4442630" alias="SC_EXP_30602_7#124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A5, constructed from sample accession ERS3498422 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGAGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L: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="127"/>
        </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="ERX4442631" alias="SC_EXP_30602_7#127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A5, constructed from sample accession ERS3498311 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTCGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498311">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694350</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A5</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="130"/>
        </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="ERX4442632" alias="SC_EXP_30602_7#128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B5, constructed from sample accession ERS3498423 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGGTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B5</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="123"/>
        </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="ERX4442633" alias="SC_EXP_30602_7#131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#131</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B5, constructed from sample accession ERS3498312 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GAGGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498312">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B5</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="130"/>
        </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="ERX4442634" alias="SC_EXP_30602_7#132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C5, constructed from sample accession ERS3498424 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTAATCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C5</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="129"/>
        </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="ERX4442635" alias="SC_EXP_30602_7#135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#135</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C5, constructed from sample accession ERS3498313 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCATGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C5</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="133"/>
        </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="ERX4442636" alias="SC_EXP_30602_7#136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D5, constructed from sample accession ERS3498427 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTTATGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D5</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="128"/>
        </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="ERX4442637" alias="SC_EXP_30602_7#139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D5, constructed from sample accession ERS3498314 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGGTACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498314">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D5</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="125"/>
        </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="ERX4442638" alias="SC_EXP_30602_7#140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E5, constructed from sample accession ERS3498428 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTATGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E5</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="122"/>
        </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="ERX4442639" alias="SC_EXP_30602_7#143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E5, constructed from sample accession ERS3498315 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTAAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E5</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="126"/>
        </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="ERX4442640" alias="SC_EXP_30602_7#144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F5, constructed from sample accession ERS3498429 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTGTTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" 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 accession="ERX4442641" alias="SC_EXP_30602_7#147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F5, constructed from sample accession ERS3498316 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGAGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F5</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="130"/>
        </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="ERX4442642" alias="SC_EXP_30602_7#148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G5, constructed from sample accession ERS3498431 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TATATTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G5</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="129"/>
        </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="ERX4442643" alias="SC_EXP_30602_7#151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#151</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G5, constructed from sample accession ERS3498317 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GACGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498317">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="123"/>
        </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="ERX4442644" alias="SC_EXP_30602_7#152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H5, constructed from sample accession ERS3498432 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGACCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H5</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="124"/>
        </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="ERX4442645" alias="SC_EXP_30602_7#155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H5, constructed from sample accession ERS3498318 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTGCTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H5</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="129"/>
        </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="ERX4442646" alias="SC_EXP_30602_7#156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442646</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A6, constructed from sample accession ERS3498433 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:A6</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="122"/>
        </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="ERX4442647" alias="SC_EXP_30602_7#159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#159</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A6, constructed from sample accession ERS3498319 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCTCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A6</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="128"/>
        </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="ERX4442648" alias="SC_EXP_30602_7#160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442648</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B6, constructed from sample accession ERS3498437 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTTGGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B6</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="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="ERX4442649" alias="SC_EXP_30602_7#163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442649</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B6, constructed from sample accession ERS3498320 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTTCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B6</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="127"/>
        </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="ERX4442650" alias="SC_EXP_30602_7#164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442650</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C6, constructed from sample accession ERS3498425 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCGAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C6</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="123"/>
        </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="ERX4442651" alias="SC_EXP_30602_7#167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442651</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#167</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C6, constructed from sample accession ERS3498321 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GATATGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C6</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="125"/>
        </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="ERX4442652" alias="SC_EXP_30602_7#168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442652</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D6, constructed from sample accession ERS3498426 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGTCGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D6</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="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="ERX4442653" alias="SC_EXP_30602_7#171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442653</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D6, constructed from sample accession ERS3498322 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D6</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="124"/>
        </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="ERX4442654" alias="SC_EXP_30602_7#172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442654</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#172</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E6, constructed from sample accession ERS3498439 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence ATCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E6</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="127"/>
        </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="ERX4442655" alias="SC_EXP_30602_7#175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442655</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E6, constructed from sample accession ERS3498323 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E6</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="130"/>
        </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="ERX4442656" alias="SC_EXP_30602_7#176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442656</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F6, constructed from sample accession ERS3498440 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TGGGCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F6</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="124"/>
        </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="ERX4442657" alias="SC_EXP_30602_7#179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442657</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#179</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F6, constructed from sample accession ERS3498324 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCTCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F6</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="128"/>
        </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="ERX4442658" alias="SC_EXP_30602_7#180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442658</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G6, constructed from sample accession ERS3498353 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGGCACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694392</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G6</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="126"/>
        </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="ERX4442659" alias="SC_EXP_30602_7#183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442659</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#183</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G6, constructed from sample accession ERS3498325 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCGGCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G6</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="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="ERX4442660" alias="SC_EXP_30602_7#184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442660</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#184</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H6, constructed from sample accession ERS3498364 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CAAATAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H6</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="124"/>
        </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="ERX4442661" alias="SC_EXP_30602_7#187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#187</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H6, constructed from sample accession ERS3498326 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CACTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H6</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="125"/>
        </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="ERX4442662" alias="SC_EXP_30602_7#188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442662</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#188</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A7, constructed from sample accession ERS3498365 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCTTCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:A7</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="125"/>
        </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="ERX4442663" alias="SC_EXP_30602_7#191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442663</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#191</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A7, constructed from sample accession ERS3498327 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTTACCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498327">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A7</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="128"/>
        </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="ERX4442664" alias="SC_EXP_30602_7#192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#192</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B7, constructed from sample accession ERS3498366 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTTAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B7</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="124"/>
        </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="ERX4442665" alias="SC_EXP_30602_7#195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#195</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B7, constructed from sample accession ERS3498328 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TACGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B7</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="126"/>
        </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="ERX4442666" alias="SC_EXP_30602_7#196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#196</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C7, constructed from sample accession ERS3498367 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AATAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C7</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="122"/>
        </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="ERX4442667" alias="SC_EXP_30602_7#199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442667</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#199</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C7, constructed from sample accession ERS3498329 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTTCGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C7</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="132"/>
        </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="ERX4442668" alias="SC_EXP_30602_7#200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442668</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#200</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D7, constructed from sample accession ERS3498373 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGTTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D7</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="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="ERX4442669" alias="SC_EXP_30602_7#203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442669</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#203</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D7, constructed from sample accession ERS3498330 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCACTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D7</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="124"/>
        </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="ERX4442670" alias="SC_EXP_30602_7#204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442670</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#204</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E7, constructed from sample accession ERS3498381 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCGTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694421</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E7</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="ERX4442671" alias="SC_EXP_30602_7#207">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442671</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#207</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E7, constructed from sample accession ERS3498331 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTGATGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E7</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="125"/>
        </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="ERX4442672" alias="SC_EXP_30602_7#208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442672</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#208</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F7, constructed from sample accession ERS3498384 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGGACTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F7</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="127"/>
        </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="ERX4442673" alias="SC_EXP_30602_7#211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#211</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F7, constructed from sample accession ERS3498332 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGGACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F7</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="128"/>
        </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="ERX4442674" alias="SC_EXP_30602_7#212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#212</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G7, constructed from sample accession ERS3498385 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTGGGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694425</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G7</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="125"/>
        </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="ERX4442675" alias="SC_EXP_30602_7#215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#215</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G7, constructed from sample accession ERS3498333 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TAGTATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="125"/>
        </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="ERX4442676" alias="SC_EXP_30602_7#216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#216</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H7, constructed from sample accession ERS3498334 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGACACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="123"/>
        </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="ERX4442677" alias="SC_EXP_30602_7#217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#217</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H7, constructed from sample accession ERS3498386 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GATATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H7</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="124"/>
        </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="ERX4442678" alias="SC_EXP_30602_7#220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#220</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A8, constructed from sample accession ERS3498335 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AGTAGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694374</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A8</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="129"/>
        </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="ERX4442679" alias="SC_EXP_30602_7#221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#221</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A8, constructed from sample accession ERS3498387 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AATGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:A8</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="131"/>
        </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="ERX4442680" alias="SC_EXP_30602_7#224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#224</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B8, constructed from sample accession ERS3498336 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GAGGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B8</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="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 accession="ERX4442681" alias="SC_EXP_30602_7#225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#225</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B8, constructed from sample accession ERS3498388 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCAATAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B8</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="130"/>
        </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="ERX4442682" alias="SC_EXP_30602_7#228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#228</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C8, constructed from sample accession ERS3498337 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTGTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C8</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="129"/>
        </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="ERX4442683" alias="SC_EXP_30602_7#229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#229</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:C8, constructed from sample accession ERS3498391 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="125"/>
        </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="ERX4442684" alias="SC_EXP_30602_7#232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#232</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D8, constructed from sample accession ERS3498338 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGCAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D8</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="122"/>
        </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="ERX4442685" alias="SC_EXP_30602_7#233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#233</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:D8, constructed from sample accession ERS3498399 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:D8</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="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="ERX4442686" alias="SC_EXP_30602_7#236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#236</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E8, constructed from sample accession ERS3498339 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTTGCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E8</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="123"/>
        </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="ERX4442687" alias="SC_EXP_30602_7#237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#237</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:E8, constructed from sample accession ERS3498402 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCCGCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498402">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:E8</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="123"/>
        </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="ERX4442688" alias="SC_EXP_30602_7#240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#240</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F8, constructed from sample accession ERS3498340 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CATATTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F8</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="126"/>
        </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="ERX4442689" alias="SC_EXP_30602_7#241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#241</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:F8, constructed from sample accession ERS3498430 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCAAACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:F8</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="125"/>
        </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="ERX4442690" alias="SC_EXP_30602_7#245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#245</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G8, constructed from sample accession ERS3498341 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTCCTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G8</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="129"/>
        </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="ERX4442691" alias="SC_EXP_30602_7#246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#246</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:G8, constructed from sample accession ERS3498434 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCCGATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:G8</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="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="ERX4442692" alias="SC_EXP_30602_7#249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#249</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H8, constructed from sample accession ERS3498342 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GACTCCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="133"/>
        </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="ERX4442693" alias="SC_EXP_30602_7#250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#250</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:H8, constructed from sample accession ERS3498435 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CACGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:H8</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="125"/>
        </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="ERX4442694" alias="SC_EXP_30602_7#253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#253</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A9, constructed from sample accession ERS3498343 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCACGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A9</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="122"/>
        </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="ERX4442695" alias="SC_EXP_30602_7#254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#254</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:A9, constructed from sample accession ERS3498436 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:A9</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="136"/>
        </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="ERX4442696" alias="SC_EXP_30602_7#257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#257</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B9, constructed from sample accession ERS3498344 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCTGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B9</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="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 accession="ERX4442697" alias="SC_EXP_30602_7#258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#258</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN539162L:B9, constructed from sample accession ERS3498438 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TCTGAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN539162L:B9</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="125"/>
        </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="ERX4442698" alias="SC_EXP_30602_7#261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#261</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C9, constructed from sample accession ERS3498345 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCAGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694384</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="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="ERX4442699" alias="SC_EXP_30602_7#265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#265</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#265</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D9, constructed from sample accession ERS3498346 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CATCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694385</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D9</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="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="ERX4442700" alias="SC_EXP_30602_7#269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#269</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E9, constructed from sample accession ERS3498347 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTGTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694386</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E9</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="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="ERX4442701" alias="SC_EXP_30602_7#273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#273</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F9, constructed from sample accession ERS3498348 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TATCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694387</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F9</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="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="ERX4442702" alias="SC_EXP_30602_7#277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#277</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#277</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G9, constructed from sample accession ERS3498349 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CACTGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694388</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G9</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="132"/>
        </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="ERX4442703" alias="SC_EXP_30602_7#281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#281</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H9, constructed from sample accession ERS3498350 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGAGTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694389</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H9</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="125"/>
        </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="ERX4442704" alias="SC_EXP_30602_7#285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#285</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A10, constructed from sample accession ERS3498351 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCGGAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442705" alias="SC_EXP_30602_7#289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#289</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#289</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B10, constructed from sample accession ERS3498352 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTGGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694391</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442706" alias="SC_EXP_30602_7#293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#293</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C10, constructed from sample accession ERS3498354 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTTCAAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="405" NOMINAL_SDEV="56"/>
        </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="ERX4442707" alias="SC_EXP_30602_7#297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#297</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D10, constructed from sample accession ERS3498355 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D10</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="142"/>
        </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="ERX4442708" alias="SC_EXP_30602_7#301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E10, constructed from sample accession ERS3498356 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCCTAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694395</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E10</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="123"/>
        </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="ERX4442709" alias="SC_EXP_30602_7#305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#305</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F10, constructed from sample accession ERS3498357 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGAGGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F10</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="138"/>
        </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="ERX4442710" alias="SC_EXP_30602_7#309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G10, constructed from sample accession ERS3498358 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GAGCGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694397</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G10</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="125"/>
        </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="ERX4442711" alias="SC_EXP_30602_7#313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H10, constructed from sample accession ERS3498359 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTCGCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694398</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H10</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="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="ERX4442712" alias="SC_EXP_30602_7#317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#317</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A11, constructed from sample accession ERS3498360 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTCTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A11</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="122"/>
        </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="ERX4442713" alias="SC_EXP_30602_7#321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B11, constructed from sample accession ERS3498361 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCAGGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694400</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" 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="ERX4442714" alias="SC_EXP_30602_7#325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#325</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C11, constructed from sample accession ERS3498362 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGTGTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="39"/>
        </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="ERX4442715" alias="SC_EXP_30602_7#329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#329</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#329</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D11, constructed from sample accession ERS3498363 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AAGGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D11</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="120"/>
        </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="ERX4442716" alias="SC_EXP_30602_7#334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#334</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#334</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E11, constructed from sample accession ERS3498368 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CTTACTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694407</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E11</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="128"/>
        </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="ERX4442717" alias="SC_EXP_30602_7#338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#338</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#338</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F11, constructed from sample accession ERS3498369 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GCGAATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="128"/>
        </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="ERX4442718" alias="SC_EXP_30602_7#342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#342</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#342</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G11, constructed from sample accession ERS3498370 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGTTTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G11</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="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 accession="ERX4442719" alias="SC_EXP_30602_7#346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#346</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#346</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H11, constructed from sample accession ERS3498371 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CCAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H11</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="128"/>
        </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="ERX4442720" alias="SC_EXP_30602_7#350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#350</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#350</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:A12, constructed from sample accession ERS3498372 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GTGAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:A12</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="125"/>
        </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="ERX4442721" alias="SC_EXP_30602_7#354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#354</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#354</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:B12, constructed from sample accession ERS3498374 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TTTGGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:B12</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="125"/>
        </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="ERX4442722" alias="SC_EXP_30602_7#358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#358</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#358</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:C12, constructed from sample accession ERS3498375 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AACAGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:C12</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="124"/>
        </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="ERX4442723" alias="SC_EXP_30602_7#362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#362</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#362</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:D12, constructed from sample accession ERS3498376 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence AATTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:D12</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="125"/>
        </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="ERX4442724" alias="SC_EXP_30602_7#366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#366</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#366</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:E12, constructed from sample accession ERS3498377 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGCATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:E12</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="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 accession="ERX4442725" alias="SC_EXP_30602_7#370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#370</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#370</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:F12, constructed from sample accession ERS3498378 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence TGTTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694417</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:F12</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="128"/>
        </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="ERX4442726" alias="SC_EXP_30602_7#374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#374</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#374</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:G12, constructed from sample accession ERS3498379 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence CGGGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:G12</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="125"/>
        </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="ERX4442727" alias="SC_EXP_30602_7#378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30602_7#378</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30602_7#378</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115362">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115362</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB32657</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN538980K:H12, constructed from sample accession ERS3498380 for study accession ERP115362.  This is part of an Illumina multiplexed sequencing run (30602_7).  This submission includes reads tagged with the sequence GGTGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3498380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3498380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5694420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN538980K:H12</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="128"/>
        </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>
