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  <EXPERIMENT accession="ERX4965797" alias="SC_EXP_32566_2#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A1, constructed from sample accession ERS3903094 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCGTTAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903094">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965798" alias="SC_EXP_32566_2#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B1, constructed from sample accession ERS3902938 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTTAACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965799" alias="SC_EXP_32566_2#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B1, constructed from sample accession ERS3903095 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCGACTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903095">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="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="ERX4965800" alias="SC_EXP_32566_2#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C1, constructed from sample accession ERS3902944 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CATTTATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965801" alias="SC_EXP_32566_2#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C1, constructed from sample accession ERS3903096 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGTAAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903096">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" 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="ERX4965802" alias="SC_EXP_32566_2#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D1, constructed from sample accession ERS3902947 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTAGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965803" alias="SC_EXP_32566_2#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D1, constructed from sample accession ERS3903097 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGTCGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965804" alias="SC_EXP_32566_2#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E1, constructed from sample accession ERS3902952 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTGATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" 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="ERX4965805" alias="SC_EXP_32566_2#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E1, constructed from sample accession ERS3903099 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTCTCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903099">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E1</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="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="ERX4965806" alias="SC_EXP_32566_2#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F1, constructed from sample accession ERS3902949 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TATTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="422" 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="ERX4965807" alias="SC_EXP_32566_2#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F1, constructed from sample accession ERS3903098 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCTCATAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A: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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965808" alias="SC_EXP_32566_2#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G1, constructed from sample accession ERS3902954 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTACGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965809" alias="SC_EXP_32566_2#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G1, constructed from sample accession ERS3903100 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCGGGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903100">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G1</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="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="ERX4965810" alias="SC_EXP_32566_2#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H1, constructed from sample accession ERS3902956 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTGATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102272</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" 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="ERX4965811" alias="SC_EXP_32566_2#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H1, constructed from sample accession ERS3903102 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGAACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903102">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="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="ERX4965812" alias="SC_EXP_32566_2#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A2, constructed from sample accession ERS3902960 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TATATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965813" alias="SC_EXP_32566_2#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A2, constructed from sample accession ERS3903103 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TGTTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903103">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965814" alias="SC_EXP_32566_2#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B2, constructed from sample accession ERS3902957 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTATCCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902957">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965815" alias="SC_EXP_32566_2#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B2, constructed from sample accession ERS3903105 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCCACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A: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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965816" alias="SC_EXP_32566_2#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C2, constructed from sample accession ERS3902958 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTACCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102274</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" 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="ERX4965817" alias="SC_EXP_32566_2#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C2, constructed from sample accession ERS3903106 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGCCTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="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="ERX4965818" alias="SC_EXP_32566_2#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D2, constructed from sample accession ERS3902964 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CAGAGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102280</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="422" 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="ERX4965819" alias="SC_EXP_32566_2#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965819</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D2, constructed from sample accession ERS3903109 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTCGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="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="ERX4965820" alias="SC_EXP_32566_2#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965820</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E2, constructed from sample accession ERS3902966 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CATCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="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="ERX4965821" alias="SC_EXP_32566_2#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965821</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E2, constructed from sample accession ERS3903110 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGACGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965822" alias="SC_EXP_32566_2#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965822</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F2, constructed from sample accession ERS3902970 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTTCCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="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="ERX4965823" alias="SC_EXP_32566_2#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965823</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F2, constructed from sample accession ERS3903111 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGTGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="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="ERX4965824" alias="SC_EXP_32566_2#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965824</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G2, constructed from sample accession ERS3903117 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTTCAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="361" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965825" alias="SC_EXP_32566_2#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965825</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G2, constructed from sample accession ERS3902969 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TAGGCGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="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="ERX4965826" alias="SC_EXP_32566_2#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965826</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H2, constructed from sample accession ERS3903115 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CACTCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A: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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965827" alias="SC_EXP_32566_2#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H2, constructed from sample accession ERS3902965 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GACTTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" 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="ERX4965828" alias="SC_EXP_32566_2#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965828</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A3, constructed from sample accession ERS3903114 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCATGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A3</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="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="ERX4965829" alias="SC_EXP_32566_2#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A3, constructed from sample accession ERS3902967 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCATCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102283</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A3</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="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="ERX4965830" alias="SC_EXP_32566_2#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965830</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B3, constructed from sample accession ERS3903113 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCTTGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B3</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="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="ERX4965831" alias="SC_EXP_32566_2#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965831</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B3, constructed from sample accession ERS3902968 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence ACTTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102284</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B3</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="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="ERX4965832" alias="SC_EXP_32566_2#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965832</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C3, constructed from sample accession ERS3903116 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGGCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C3</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="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="ERX4965833" alias="SC_EXP_32566_2#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965833</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C3, constructed from sample accession ERS3902971 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCTAAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965834" alias="SC_EXP_32566_2#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965834</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D3, constructed from sample accession ERS3903118 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGTTCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D3</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="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="ERX4965835" alias="SC_EXP_32566_2#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965835</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D3, constructed from sample accession ERS3902974 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102290</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="253"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965836" alias="SC_EXP_32566_2#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965836</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E3, constructed from sample accession ERS3903120 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTATATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="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="ERX4965837" alias="SC_EXP_32566_2#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965837</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E3, constructed from sample accession ERS3902975 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTCCGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="19"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965838" alias="SC_EXP_32566_2#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965838</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F3, constructed from sample accession ERS3902983 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCGCTAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102299</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="324" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965839" alias="SC_EXP_32566_2#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965839</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F3, constructed from sample accession ERS3903122 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCTAAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F3</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="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="ERX4965840" alias="SC_EXP_32566_2#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965840</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G3, constructed from sample accession ERS3902985 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCCACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102301</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965841" alias="SC_EXP_32566_2#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965841</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G3, constructed from sample accession ERS3903121 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCGCCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965842" alias="SC_EXP_32566_2#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965842</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H3, constructed from sample accession ERS4043057 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AACTTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4043057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4043057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6243376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" 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="ERX4965843" alias="SC_EXP_32566_2#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H3, constructed from sample accession ERS3903125 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGCTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H3</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="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="ERX4965844" alias="SC_EXP_32566_2#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965844</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A4, constructed from sample accession ERS4043058 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTAACTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4043058">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4043058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6243377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965845" alias="SC_EXP_32566_2#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965845</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A4, constructed from sample accession ERS3903123 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CACCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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="ERX4965846" alias="SC_EXP_32566_2#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965846</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B4, constructed from sample accession ERS3902988 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTGCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965847" alias="SC_EXP_32566_2#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B4, constructed from sample accession ERS3903126 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGCTGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" 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="ERX4965848" alias="SC_EXP_32566_2#53">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965848</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C4, constructed from sample accession ERS3902996 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTTAGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965849" alias="SC_EXP_32566_2#54">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965849</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C4, constructed from sample accession ERS3903127 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence ACGTTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="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="ERX4965850" alias="SC_EXP_32566_2#55">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965850</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D4, constructed from sample accession ERS3902997 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGTGGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102313</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965851" alias="SC_EXP_32566_2#56">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965851</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D4, constructed from sample accession ERS3903130 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGCTTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" 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="ERX4965852" alias="SC_EXP_32566_2#57">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965852</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E4, constructed from sample accession ERS3902993 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence ATATGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102309</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965853" alias="SC_EXP_32566_2#58">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965853</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E4, constructed from sample accession ERS3903131 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGACGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="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="ERX4965854" alias="SC_EXP_32566_2#59">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965854</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F4, constructed from sample accession ERS3902995 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965855" alias="SC_EXP_32566_2#60">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#60</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F4, constructed from sample accession ERS3903132 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTGCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F4</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="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="ERX4965856" alias="SC_EXP_32566_2#61">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G4, constructed from sample accession ERS3902994 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGCCTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102310</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965857" alias="SC_EXP_32566_2#62">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G4, constructed from sample accession ERS3903137 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGCATCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="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="ERX4965858" alias="SC_EXP_32566_2#63">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H4, constructed from sample accession ERS3903001 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGATAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903001">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903001</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965859" alias="SC_EXP_32566_2#64">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H4, constructed from sample accession ERS3903134 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CACGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H4</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="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="ERX4965860" alias="SC_EXP_32566_2#65">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A5, constructed from sample accession ERS3902999 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTCGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902999">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902999</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102315</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965861" alias="SC_EXP_32566_2#66">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965861</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A5, constructed from sample accession ERS3903135 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGAGCAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A5</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="ERX4965862" alias="SC_EXP_32566_2#67">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B5, constructed from sample accession ERS3903005 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GAGGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903005">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="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="ERX4965863" alias="SC_EXP_32566_2#68">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965863</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B5, constructed from sample accession ERS3903136 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGGTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" 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="ERX4965864" alias="SC_EXP_32566_2#69">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965864</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C5, constructed from sample accession ERS3903003 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCATGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903003">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102319</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C5</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="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="ERX4965865" alias="SC_EXP_32566_2#70">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965865</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C5, constructed from sample accession ERS3903138 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTAATCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903138">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="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="ERX4965866" alias="SC_EXP_32566_2#71">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965866</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D5, constructed from sample accession ERS3903141 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTATGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903141">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" 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="ERX4965867" alias="SC_EXP_32566_2#72">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965867</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D5, constructed from sample accession ERS3903000 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGGTACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965868" alias="SC_EXP_32566_2#73">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965868</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E5, constructed from sample accession ERS3903140 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTATGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903140">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="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="ERX4965869" alias="SC_EXP_32566_2#74">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965869</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E5, constructed from sample accession ERS3903004 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTAAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903004">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903004</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E5</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="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="ERX4965870" alias="SC_EXP_32566_2#75">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965870</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F5, constructed from sample accession ERS3903139 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTGTTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903139">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" 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="ERX4965871" alias="SC_EXP_32566_2#76">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965871</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F5, constructed from sample accession ERS3903007 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGAGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903007">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903007</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="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="ERX4965872" alias="SC_EXP_32566_2#77">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965872</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G5, constructed from sample accession ERS3903142 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TATATTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903142">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965873" alias="SC_EXP_32566_2#78">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965873</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G5, constructed from sample accession ERS3903008 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GACGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102324</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" 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="ERX4965874" alias="SC_EXP_32566_2#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965874</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H5, constructed from sample accession ERS3903144 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGACCATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903144">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="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="ERX4965875" alias="SC_EXP_32566_2#80">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965875</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H5, constructed from sample accession ERS3903009 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTGCTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903009">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102325</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="422" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965876" alias="SC_EXP_32566_2#81">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965876</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A6, constructed from sample accession ERS3903143 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903143">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="358" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965877" alias="SC_EXP_32566_2#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965877</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A6, constructed from sample accession ERS3903010 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCTCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="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="ERX4965878" alias="SC_EXP_32566_2#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B6, constructed from sample accession ERS3903149 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTGGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903149">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B6</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="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="ERX4965879" alias="SC_EXP_32566_2#84">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B6, constructed from sample accession ERS3903017 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903017">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965880" alias="SC_EXP_32566_2#85">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965880</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C6, constructed from sample accession ERS3903012 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GATATGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903012">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102328</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" 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="ERX4965881" alias="SC_EXP_32566_2#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965881</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C6, constructed from sample accession ERS3903146 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCGAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903146">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C6</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="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="ERX4965882" alias="SC_EXP_32566_2#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965882</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D6, constructed from sample accession ERS3903018 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" 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="ERX4965883" alias="SC_EXP_32566_2#88">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965883</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D6, constructed from sample accession ERS3903147 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGTCGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965884" alias="SC_EXP_32566_2#89">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965884</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E6, constructed from sample accession ERS3903013 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903013">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="360" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965885" alias="SC_EXP_32566_2#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965885</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E6, constructed from sample accession ERS3903150 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence ATCAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" 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="ERX4965886" alias="SC_EXP_32566_2#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965886</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F6, constructed from sample accession ERS3903014 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCTCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F6</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="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="ERX4965887" alias="SC_EXP_32566_2#92">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965887</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F6, constructed from sample accession ERS3903148 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TGGGCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903148">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="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="ERX4965888" alias="SC_EXP_32566_2#93">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965888</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G6, constructed from sample accession ERS3903019 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCGGCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903019">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" 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="ERX4965889" alias="SC_EXP_32566_2#94">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965889</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G6, constructed from sample accession ERS3903151 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGGCACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903151">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="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="ERX4965890" alias="SC_EXP_32566_2#95">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965890</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#95</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H6, constructed from sample accession ERS3903021 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CACTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102337</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965891" alias="SC_EXP_32566_2#96">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965891</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H6, constructed from sample accession ERS3903152 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CAAATAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903152">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H6</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="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="ERX4965892" alias="SC_EXP_32566_2#97">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965892</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#97</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A7, constructed from sample accession ERS3903022 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTACCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903022">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102338</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A7</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="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="ERX4965893" alias="SC_EXP_32566_2#98">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965893</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A7, constructed from sample accession ERS3903153 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCTTCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903153">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A7</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="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="ERX4965894" alias="SC_EXP_32566_2#99">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965894</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B7, constructed from sample accession ERS3903023 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TACGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903023">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B7</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="ERX4965895" alias="SC_EXP_32566_2#100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965895</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B7, constructed from sample accession ERS3903154 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903154">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="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="ERX4965896" alias="SC_EXP_32566_2#101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965896</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#101</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C7, constructed from sample accession ERS3903024 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTTCGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965897" alias="SC_EXP_32566_2#102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965897</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#102</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C7, constructed from sample accession ERS3903155 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AATAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903155">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965898" alias="SC_EXP_32566_2#103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965898</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D7, constructed from sample accession ERS3903025 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCACTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903025">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102341</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="354" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965899" alias="SC_EXP_32566_2#104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965899</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D7, constructed from sample accession ERS3903156 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGTTCGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903156">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="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="ERX4965900" alias="SC_EXP_32566_2#105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965900</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E7, constructed from sample accession ERS3903026 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTGATGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903026">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102342</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965901" alias="SC_EXP_32566_2#106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965901</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E7, constructed from sample accession ERS3903157 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCGTGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903157">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" 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="ERX4965902" alias="SC_EXP_32566_2#107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965902</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#107</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F7, constructed from sample accession ERS3903030 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGGACAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102346</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" 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="ERX4965903" alias="SC_EXP_32566_2#108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965903</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F7, constructed from sample accession ERS3903158 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGGACTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903158">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="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="ERX4965904" alias="SC_EXP_32566_2#109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965904</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G7, constructed from sample accession ERS3903029 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TAGTATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102345</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" 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="ERX4965905" alias="SC_EXP_32566_2#110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965905</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G7, constructed from sample accession ERS3903164 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTGGGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="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="ERX4965906" alias="SC_EXP_32566_2#111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965906</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H7, constructed from sample accession ERS3903159 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GATATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903159">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="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="ERX4965907" alias="SC_EXP_32566_2#112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965907</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H7, constructed from sample accession ERS3903028 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGACACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903028">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="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="ERX4965908" alias="SC_EXP_32566_2#113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965908</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#113</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A8, constructed from sample accession ERS3903160 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AATGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903160">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903160</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" 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="ERX4965909" alias="SC_EXP_32566_2#114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A8, constructed from sample accession ERS3903031 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AGTAGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903031">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102347</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A8</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="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="ERX4965910" alias="SC_EXP_32566_2#115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B8, constructed from sample accession ERS3903161 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCAATAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903161">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="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="ERX4965911" alias="SC_EXP_32566_2#116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#116</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B8, constructed from sample accession ERS3903032 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GAGGGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="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="ERX4965912" alias="SC_EXP_32566_2#117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#117</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C8, constructed from sample accession ERS3903163 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903163">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C8</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="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="ERX4965913" alias="SC_EXP_32566_2#118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#118</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C8, constructed from sample accession ERS3903033 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTGTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C8</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="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="ERX4965914" alias="SC_EXP_32566_2#119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#119</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D8, constructed from sample accession ERS3903162 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCGTAAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903162">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903162</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965915" alias="SC_EXP_32566_2#120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965915</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#120</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D8, constructed from sample accession ERS3903034 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGCAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903034">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102350</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965916" alias="SC_EXP_32566_2#121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#121</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E8, constructed from sample accession ERS3903168 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCCGCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903168">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965917" alias="SC_EXP_32566_2#122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E8, constructed from sample accession ERS3903039 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTTGCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" 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="ERX4965918" alias="SC_EXP_32566_2#123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F8, constructed from sample accession ERS3903174 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCAAACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903174">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="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="ERX4965919" alias="SC_EXP_32566_2#124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F8, constructed from sample accession ERS3903035 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CATATTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903035">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965920" alias="SC_EXP_32566_2#125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#125</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G8, constructed from sample accession ERS3903036 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTCCTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="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="ERX4965921" alias="SC_EXP_32566_2#126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#126</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G8, constructed from sample accession ERS3903172 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCCGATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903172">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="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="ERX4965922" alias="SC_EXP_32566_2#127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H8, constructed from sample accession ERS3903040 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GACTCCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903040">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965923" alias="SC_EXP_32566_2#128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H8, constructed from sample accession ERS3903175 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CACGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903175">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102492</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" 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="ERX4965924" alias="SC_EXP_32566_2#129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#129</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A9, constructed from sample accession ERS3903038 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCACGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903038">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A9</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965925" alias="SC_EXP_32566_2#130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#130</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A9, constructed from sample accession ERS3903177 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903177">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" 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="ERX4965926" alias="SC_EXP_32566_2#131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#131</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B9, constructed from sample accession ERS3903037 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCTGGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903037">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="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="ERX4965927" alias="SC_EXP_32566_2#132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B9, constructed from sample accession ERS3903179 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCTGAATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903179">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="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="ERX4965928" alias="SC_EXP_32566_2#133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#133</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C9, constructed from sample accession ERS3903042 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCAGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" 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="ERX4965929" alias="SC_EXP_32566_2#134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965929</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#134</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C9, constructed from sample accession ERS3903180 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGGAAAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903180">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903180</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965930" alias="SC_EXP_32566_2#135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965930</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#135</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D9, constructed from sample accession ERS3903041 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CATCGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903041">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965931" alias="SC_EXP_32566_2#136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965931</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D9, constructed from sample accession ERS3903183 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTGGTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903183">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903183</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965932" alias="SC_EXP_32566_2#137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#137</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E9, constructed from sample accession ERS3903043 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTGTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E9</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="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="ERX4965933" alias="SC_EXP_32566_2#138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965933</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#138</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E9, constructed from sample accession ERS3903184 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903184">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965934" alias="SC_EXP_32566_2#139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F9, constructed from sample accession ERS3903045 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TATCGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903045">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965935" alias="SC_EXP_32566_2#140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F9, constructed from sample accession ERS3903187 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCAGTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903187">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965936" alias="SC_EXP_32566_2#141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965936</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#141</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G9, constructed from sample accession ERS3903047 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CACTGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965937" alias="SC_EXP_32566_2#142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965937</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#142</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G9, constructed from sample accession ERS3903188 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTGGGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903188">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" 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="ERX4965938" alias="SC_EXP_32566_2#143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H9, constructed from sample accession ERS3903049 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGAGTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965939" alias="SC_EXP_32566_2#144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H9, constructed from sample accession ERS3903186 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGGACCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903186">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965940" alias="SC_EXP_32566_2#145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#145</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A10, constructed from sample accession ERS3903052 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCGGAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965941" alias="SC_EXP_32566_2#146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#146</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A10, constructed from sample accession ERS3903191 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTTGACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903191">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965942" alias="SC_EXP_32566_2#147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B10, constructed from sample accession ERS3903051 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTGGGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903051">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="423" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965943" alias="SC_EXP_32566_2#148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B10, constructed from sample accession ERS3903192 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGGGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903192">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903192</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102509</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965944" alias="SC_EXP_32566_2#149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#149</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C10, constructed from sample accession ERS3903054 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTTCAAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903054">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="440" NOMINAL_SDEV="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="ERX4965945" alias="SC_EXP_32566_2#150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#150</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C10, constructed from sample accession ERS3903194 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GAGACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903194">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903194</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102511</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="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="ERX4965946" alias="SC_EXP_32566_2#151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#151</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D10, constructed from sample accession ERS3903056 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965947" alias="SC_EXP_32566_2#152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D10, constructed from sample accession ERS3903193 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCCAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903193">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903193</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102510</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="324"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965948" alias="SC_EXP_32566_2#153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#153</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E10, constructed from sample accession ERS3903201 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGCGTTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903201">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903201</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965949" alias="SC_EXP_32566_2#154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#154</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E10, constructed from sample accession ERS3903057 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCCTAGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965950" alias="SC_EXP_32566_2#155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F10, constructed from sample accession ERS3903203 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGTAGTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903203">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903203</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965951" alias="SC_EXP_32566_2#156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F10, constructed from sample accession ERS3903058 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGAGGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903058">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102374</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F10</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965952" alias="SC_EXP_32566_2#157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#157</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G10, constructed from sample accession ERS3902951 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence ACGCGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102267</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" 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="ERX4965953" alias="SC_EXP_32566_2#158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#158</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G10, constructed from sample accession ERS3903060 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GAGCGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903060">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903060</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="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="ERX4965954" alias="SC_EXP_32566_2#159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#159</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H10, constructed from sample accession ERS3902953 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTGACTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3902953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3902953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="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="ERX4965955" alias="SC_EXP_32566_2#160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H10, constructed from sample accession ERS3903062 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTCGCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903062">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903062</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="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="ERX4965956" alias="SC_EXP_32566_2#161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#161</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A11, constructed from sample accession ERS4043059 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTTTGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4043059">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4043059</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6243378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965957" alias="SC_EXP_32566_2#162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#162</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A11, constructed from sample accession ERS3903063 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTCTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903063">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903063</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965958" alias="SC_EXP_32566_2#163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B11, constructed from sample accession ERS3903006 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102322</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="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="ERX4965959" alias="SC_EXP_32566_2#164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B11, constructed from sample accession ERS3903064 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCAGGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903064">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903064</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" 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="ERX4965960" alias="SC_EXP_32566_2#165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#165</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C11, constructed from sample accession ERS3903016 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTTTAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965961" alias="SC_EXP_32566_2#166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#166</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C11, constructed from sample accession ERS3903065 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGTGTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903065">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903065</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="356" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965962" alias="SC_EXP_32566_2#167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#167</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D11, constructed from sample accession ERS3903066 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AAGGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903066">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903066</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965963" alias="SC_EXP_32566_2#168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D11, constructed from sample accession ERS3903027 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TGTAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="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="ERX4965964" alias="SC_EXP_32566_2#169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#169</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E11, constructed from sample accession ERS3903070 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTTACTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903070">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903070</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102386</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965965" alias="SC_EXP_32566_2#170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#170</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E11, constructed from sample accession ERS3903044 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTCACGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903044">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E11</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="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="ERX4965966" alias="SC_EXP_32566_2#171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F11, constructed from sample accession ERS3903067 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GCGAATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903067">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903067</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="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="ERX4965967" alias="SC_EXP_32566_2#172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#172</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F11, constructed from sample accession ERS3903046 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GATGAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965968" alias="SC_EXP_32566_2#173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#173</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G11, constructed from sample accession ERS3903074 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGTTTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903074">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903074</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965969" alias="SC_EXP_32566_2#174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#174</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G11, constructed from sample accession ERS3903048 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGCGCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903048">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="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="ERX4965970" alias="SC_EXP_32566_2#175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H11, constructed from sample accession ERS3903075 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903075">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903075</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102391</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="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="ERX4965971" alias="SC_EXP_32566_2#176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:H11, constructed from sample accession ERS3903053 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AACCTGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:H11</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="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="ERX4965972" alias="SC_EXP_32566_2#177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#177</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:A12, constructed from sample accession ERS3903076 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GTGAAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903076">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903076</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102392</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="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="ERX4965973" alias="SC_EXP_32566_2#178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#178</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:A12, constructed from sample accession ERS3903059 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGTTAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903059">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903059</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="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="ERX4965974" alias="SC_EXP_32566_2#179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#179</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:B12, constructed from sample accession ERS3903077 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TTTGGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903077">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903077</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:B12</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="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="ERX4965975" alias="SC_EXP_32566_2#180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:B12, constructed from sample accession ERS3903061 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGGGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903061">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903061</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="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="ERX4965976" alias="SC_EXP_32566_2#181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#181</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:C12, constructed from sample accession ERS3903078 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AACAGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903078">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903078</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965977" alias="SC_EXP_32566_2#182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#182</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:C12, constructed from sample accession ERS3903119 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CTTGTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:C12</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="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="ERX4965978" alias="SC_EXP_32566_2#183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#183</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:D12, constructed from sample accession ERS3903089 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AATTTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903089">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965979" alias="SC_EXP_32566_2#184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#184</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:D12, constructed from sample accession ERS3903170 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence AAAGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903170">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="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="ERX4965980" alias="SC_EXP_32566_2#185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#185</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:E12, constructed from sample accession ERS3903090 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGCATGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903090">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" 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="ERX4965981" alias="SC_EXP_32566_2#186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#186</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:E12, constructed from sample accession ERS3903185 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TCAGTTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903185">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:E12</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="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="ERX4965982" alias="SC_EXP_32566_2#187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#187</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:F12, constructed from sample accession ERS3903091 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence TGTTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903091">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102407</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" 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="ERX4965983" alias="SC_EXP_32566_2#188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965983</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#188</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:F12, constructed from sample accession ERS3903195 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGGTCCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903195">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4965984" alias="SC_EXP_32566_2#189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#189</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:G12, constructed from sample accession ERS3903092 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CGGGAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903092">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:G12</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="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="ERX4965985" alias="SC_EXP_32566_2#190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#190</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN536600A:G12, constructed from sample accession ERS3903198 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence CCAGCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903198">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903198</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN536600A:G12</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="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="ERX4965986" alias="SC_EXP_32566_2#191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4965986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_32566_2#191</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_32566_2#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP009685">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP009685</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB8667</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN543962Q:H12, constructed from sample accession ERS3903093 for study accession ERP009685.  This is part of an Illumina multiplexed sequencing run (32566_2).  This submission includes reads tagged with the sequence GGTGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3903093">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3903093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA6102409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN543962Q:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="105"/>
        </LIBRARY_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>
