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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX11923421" alias="SC_EXP_46643_2#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923421</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:H4, constructed from sample accession ERS13642371 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence AGATAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="145" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923430" alias="SC_EXP_46643_2#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923430</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:A6, constructed from sample accession ERS13642380 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CCTCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923394" alias="SC_EXP_46643_2#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923394</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:E1, constructed from sample accession ERS13642373 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTGATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532331</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="134" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923419" alias="SC_EXP_46643_2#59" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923419</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:F4, constructed from sample accession ERS13642369 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CCACGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532327</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="145" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923404" alias="SC_EXP_46643_2#29" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923404</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:G2, constructed from sample accession ERS13642350 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TAGGCGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532308</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923406" alias="SC_EXP_46643_2#33" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923406</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:A3, constructed from sample accession ERS13642352 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GCATCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532310</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="136" NOMINAL_SDEV="29"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923469" alias="SC_EXP_46673_2#106" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923469</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:B8, constructed from sample accession ERS13642420 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CCTCACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="141" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923429" alias="SC_EXP_46643_2#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923429</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:H5, constructed from sample accession ERS13642379 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GTGCTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532337</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="150" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923398" alias="SC_EXP_46643_2#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923398</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:A2, constructed from sample accession ERS13642393 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TATATACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="117" NOMINAL_SDEV="19"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923471" alias="SC_EXP_46673_2#108" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923471</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:D8, constructed from sample accession ERS13642423 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GCTCTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="135" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923465" alias="SC_EXP_46673_2#102" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923465</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:F7, constructed from sample accession ERS13642417 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TGTTCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="132" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923428" alias="SC_EXP_46643_2#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923428</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:G5, constructed from sample accession ERS13642381 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GACGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532338</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="129" NOMINAL_SDEV="25"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923401" alias="SC_EXP_46643_2#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923401</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:D2, constructed from sample accession ERS13642347 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CAGAGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532305</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="136" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923399" alias="SC_EXP_46643_2#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923399</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:B2, constructed from sample accession ERS13642345 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTATCCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="135" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923440" alias="SC_EXP_46643_2#99" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923440</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:C7, constructed from sample accession ERS13642395 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CTTCGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923437" alias="SC_EXP_46643_2#96" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923437</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:H6, constructed from sample accession ERS13642389 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CACTGCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532347</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="145" NOMINAL_SDEV="35"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923432" alias="SC_EXP_46643_2#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923432</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:C6, constructed from sample accession ERS13642383 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GATATGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532341</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="138" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923410" alias="SC_EXP_46643_2#41" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923410</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:E3, constructed from sample accession ERS13642357 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CTCCGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="129" NOMINAL_SDEV="23"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923427" alias="SC_EXP_46643_2#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923427</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:F5, constructed from sample accession ERS13642378 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GGAGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532336</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="141" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923442" alias="SC_EXP_46673_2#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923442</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882001K:A1, constructed from sample accession ERS13642424 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882001K:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="138" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923392" alias="SC_EXP_46643_2#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923392</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:C1, constructed from sample accession ERS13642364 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CATTTATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532322</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="130" NOMINAL_SDEV="27"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923423" alias="SC_EXP_46643_2#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923423</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:B5, constructed from sample accession ERS13642375 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GAGGTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="135" NOMINAL_SDEV="27"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923448" alias="SC_EXP_46673_2#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923448</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:E5, constructed from sample accession ERS13642399 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CCTAGGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="35"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923417" alias="SC_EXP_46643_2#55" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923417</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:D4, constructed from sample accession ERS13642366 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GGTGGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532325</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="145" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923444" alias="SC_EXP_46673_2#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923444</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:A5, constructed from sample accession ERS13642396 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CTCTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="129" NOMINAL_SDEV="25"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923438" alias="SC_EXP_46643_2#97" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923438</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:A7, constructed from sample accession ERS13642392 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTTACCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642392">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532350</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="137" NOMINAL_SDEV="31"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923463" alias="SC_EXP_46673_2#100" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923463</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:D7, constructed from sample accession ERS13642415 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GACGCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532374</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="134" NOMINAL_SDEV="29"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923408" alias="SC_EXP_46643_2#37" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923408</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:C3, constructed from sample accession ERS13642355 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CCTAAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532313</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="143" NOMINAL_SDEV="34"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923425" alias="SC_EXP_46643_2#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923425</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:D5, constructed from sample accession ERS13642376 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CGGTACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="141" NOMINAL_SDEV="34"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923402" alias="SC_EXP_46643_2#25" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923402</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:E2, constructed from sample accession ERS13642348 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CATCATTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="135" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923434" alias="SC_EXP_46643_2#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923434</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:E6, constructed from sample accession ERS13642386 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="140" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923461" alias="SC_EXP_46673_2#98" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923461</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:B7, constructed from sample accession ERS13642418 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GGTTGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923447" alias="SC_EXP_46673_2#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923447</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:D5, constructed from sample accession ERS13642400 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TCCATTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923458" alias="SC_EXP_46673_2#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923458</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:G6, constructed from sample accession ERS13642411 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TCCTTAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="139" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923460" alias="SC_EXP_46673_2#97" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923460</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:A7, constructed from sample accession ERS13642413 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CTGAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="134" NOMINAL_SDEV="29"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923414" alias="SC_EXP_46643_2#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923414</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:A4, constructed from sample accession ERS13642361 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CTAACTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532321</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="139" NOMINAL_SDEV="29"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923450" alias="SC_EXP_46673_2#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923450</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:G5, constructed from sample accession ERS13642401 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence ACTGCGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="139" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923397" alias="SC_EXP_46643_2#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923397</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:H1, constructed from sample accession ERS13642388 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GTGATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532346</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="35"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923390" alias="SC_EXP_46643_2#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923390</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:A1, constructed from sample accession ERS13642358 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CGGAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532316</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923464" alias="SC_EXP_46673_2#101" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923464</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:E7, constructed from sample accession ERS13642416 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GGCTTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="136" NOMINAL_SDEV="31"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923411" alias="SC_EXP_46643_2#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923411</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:F3, constructed from sample accession ERS13642356 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CCGCTAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532315</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="121" NOMINAL_SDEV="20"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923457" alias="SC_EXP_46673_2#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923457</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:F6, constructed from sample accession ERS13642408 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GGGTTGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="137" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923422" alias="SC_EXP_46643_2#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923422</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:A5, constructed from sample accession ERS13642372 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CTCGGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="143" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923459" alias="SC_EXP_46673_2#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923459</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:H6, constructed from sample accession ERS13642410 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CAGAAATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="38"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923415" alias="SC_EXP_46643_2#51" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923415</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:B4, constructed from sample accession ERS13642363 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTTGCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="130" NOMINAL_SDEV="25"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923420" alias="SC_EXP_46643_2#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923420</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:G4, constructed from sample accession ERS13642370 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence AGCCTGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532328</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="137" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923453" alias="SC_EXP_46673_2#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923453</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:B6, constructed from sample accession ERS13642405 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CAAAGCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642405">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="140" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923452" alias="SC_EXP_46673_2#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923452</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:A6, constructed from sample accession ERS13642406 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TTTAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642406">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="38"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923424" alias="SC_EXP_46643_2#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923424</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:C5, constructed from sample accession ERS13642374 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GCATGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="34"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923449" alias="SC_EXP_46673_2#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923449</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:F5, constructed from sample accession ERS13642403 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TTCCAAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="38"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923466" alias="SC_EXP_46673_2#103" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923466</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:G7, constructed from sample accession ERS13642426 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GAGCACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532384</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="148" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923426" alias="SC_EXP_46643_2#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923426</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:E5, constructed from sample accession ERS13642377 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GTAAATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="138" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923455" alias="SC_EXP_46673_2#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923455</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:D6, constructed from sample accession ERS13642409 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TGAAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="145" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923418" alias="SC_EXP_46643_2#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923418</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:E4, constructed from sample accession ERS13642368 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence ATATGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="35"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923395" alias="SC_EXP_46643_2#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923395</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:F1, constructed from sample accession ERS13642385 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TATTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532345</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="130" NOMINAL_SDEV="26"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923393" alias="SC_EXP_46643_2#7" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923393</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:D1, constructed from sample accession ERS13642365 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTAGCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="135" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923413" alias="SC_EXP_46643_2#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923413</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:H3, constructed from sample accession ERS13642360 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence AACTTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532318</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="132" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923445" alias="SC_EXP_46673_2#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923445</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:B5, constructed from sample accession ERS13642397 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GAGAGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="152" NOMINAL_SDEV="41"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923468" alias="SC_EXP_46673_2#105" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923468</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:A8, constructed from sample accession ERS13642422 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GAGGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923451" alias="SC_EXP_46673_2#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923451</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:H5, constructed from sample accession ERS13642404 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GGAGGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="122" NOMINAL_SDEV="20"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923441" alias="SC_EXP_46643_2#100" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923441</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:D7, constructed from sample accession ERS13642402 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GCACTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642402">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="118" NOMINAL_SDEV="19"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923416" alias="SC_EXP_46643_2#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923416</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:C4, constructed from sample accession ERS13642367 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CTTAGAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532324</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="137" NOMINAL_SDEV="30"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923407" alias="SC_EXP_46643_2#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923407</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:B3, constructed from sample accession ERS13642353 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence ACTTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923439" alias="SC_EXP_46643_2#98" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923439</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:B7, constructed from sample accession ERS13642394 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TACGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="147" NOMINAL_SDEV="37"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923467" alias="SC_EXP_46673_2#104" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923467</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:H7, constructed from sample accession ERS13642419 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="34"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923391" alias="SC_EXP_46643_2#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923391</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:B1, constructed from sample accession ERS13642362 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GTTAACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532319</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="138" NOMINAL_SDEV="31"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923470" alias="SC_EXP_46673_2#107" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923470</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:C8, constructed from sample accession ERS13642421 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TGGCTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="126" NOMINAL_SDEV="23"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923405" alias="SC_EXP_46643_2#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923405</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:H2, constructed from sample accession ERS13642351 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GACTTATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532309</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="129" NOMINAL_SDEV="25"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923403" alias="SC_EXP_46643_2#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923403</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:F2, constructed from sample accession ERS13642349 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GTTCCGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="140" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923433" alias="SC_EXP_46643_2#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923433</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:D6, constructed from sample accession ERS13642390 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="149" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923400" alias="SC_EXP_46643_2#21" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923400</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:C2, constructed from sample accession ERS13642346 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GTACCAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="142" NOMINAL_SDEV="34"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923396" alias="SC_EXP_46643_2#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923396</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:G1, constructed from sample accession ERS13642384 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTACGCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532342</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="143" NOMINAL_SDEV="37"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923436" alias="SC_EXP_46643_2#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923436</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:G6, constructed from sample accession ERS13642391 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CCGGCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="139" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923446" alias="SC_EXP_46673_2#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923446</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:C5, constructed from sample accession ERS13642398 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence GGAAACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923412" alias="SC_EXP_46643_2#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923412</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:G3, constructed from sample accession ERS13642359 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TCCACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="133" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923431" alias="SC_EXP_46643_2#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923431</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:B6, constructed from sample accession ERS13642382 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence TTTCCAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="144" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923435" alias="SC_EXP_46643_2#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923435</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:F6, constructed from sample accession ERS13642387 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence CCTCTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="146" NOMINAL_SDEV="38"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923443" alias="SC_EXP_46673_2#3" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923443</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882001K:B1, constructed from sample accession ERS13642425 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882001K:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="137" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923454" alias="SC_EXP_46673_2#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923454</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:C6, constructed from sample accession ERS13642412 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence AGACGTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="137" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923409" alias="SC_EXP_46643_2#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923409</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_2#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881077D:D3, constructed from sample accession ERS13642354 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46643_2).  This submission includes reads tagged with the sequence GGCTCGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881077D:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="160" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923456" alias="SC_EXP_46673_2#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923456</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:E6, constructed from sample accession ERS13642407 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TTCCGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642407">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="135" NOMINAL_SDEV="29"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11923462" alias="SC_EXP_46673_2#99" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923462</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46673_2#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP141158">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP141158</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB56230</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881680Q:C7, constructed from sample accession ERS13642414 for study accession ERP141158.  This is part of an Illumina multiplexed sequencing run (46673_2).  This submission includes reads tagged with the sequence TGGGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13642414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13642414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111532372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881680Q:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="125" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Agilent Pulldown</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
