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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX11923667" alias="SC_EXP_46643_3#102" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923667</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881797F:B8, constructed from sample accession ERS14362516 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CCTCACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362516">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362516</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881797F:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="127" 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="ERX11923653" alias="SC_EXP_46643_3#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923653</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:B5, constructed from sample accession ERS14362563 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence ACGTTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362563">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362563</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251706</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="44"/>
        </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="ERX11923648" alias="SC_EXP_46643_3#58" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923648</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:E4, constructed from sample accession ERS14362558 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CGCGATAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362558">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362558</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" 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="ERX11923625" alias="SC_EXP_46643_3#12" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923625</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:F1, constructed from sample accession ERS14362523 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GTCGATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362523">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362523</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251666</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:F1</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="ERX11923661" alias="SC_EXP_46643_3#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923661</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:B6, constructed from sample accession ERS14362568 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CCAAAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362568">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362568</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251711</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="156" NOMINAL_SDEV="43"/>
        </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="ERX11923637" alias="SC_EXP_46643_3#36" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923637</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:B3, constructed from sample accession ERS14362535 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TCCTATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362535">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362535</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="151" 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="ERX11923626" alias="SC_EXP_46643_3#13" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923626</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:G1, constructed from sample accession ERS14362524 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GAGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362524">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362524</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251667</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="162" NOMINAL_SDEV="46"/>
        </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="ERX11923638" alias="SC_EXP_46643_3#38" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923638</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:C3, constructed from sample accession ERS14362547 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TTTGCTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362547">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362547</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251690</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="44"/>
        </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="ERX11923624" alias="SC_EXP_46643_3#10" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923624</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:E1, constructed from sample accession ERS14362521 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GGTTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362521">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362521</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251664</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:E1</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="ERX11923630" alias="SC_EXP_46643_3#22" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923630</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:C2, constructed from sample accession ERS14362528 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GTCAATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362528">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362528</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251671</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:C2</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="ERX11923657" alias="SC_EXP_46643_3#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923657</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:F5, constructed from sample accession ERS14362566 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TGTCGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362566">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362566</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153" NOMINAL_SDEV="44"/>
        </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="ERX11923634" alias="SC_EXP_46643_3#30" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923634</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:G2, constructed from sample accession ERS14362532 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CTCCAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362532">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362532</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:G2</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="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="ERX11923651" alias="SC_EXP_46643_3#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923651</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:H4, constructed from sample accession ERS14362560 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CTAGATAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362560">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362560</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:H4</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="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="ERX11923659" alias="SC_EXP_46643_3#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923659</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:H5, constructed from sample accession ERS14362569 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence AACCAACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362569">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362569</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251712</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="156" 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="ERX11923668" alias="SC_EXP_46643_3#103" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923668</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881797F:C8, constructed from sample accession ERS14362517 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TGGCTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362517">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881797F:C8</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="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="ERX11923658" alias="SC_EXP_46643_3#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923658</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:G5, constructed from sample accession ERS14362567 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CTTTACTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362567">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362567</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:G5</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="ERX11923636" alias="SC_EXP_46643_3#34" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923636</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:A3, constructed from sample accession ERS14362534 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence ACGCCGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362534">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362534</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251676</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153" 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="ERX11923665" alias="SC_EXP_46643_3#100" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923665</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881797F:H7, constructed from sample accession ERS14362514 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362514">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251657</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881797F:H7</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="ERX11923646" alias="SC_EXP_46643_3#54" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923646</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:C4, constructed from sample accession ERS14362555 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TGCAAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362555">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362555</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" 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="ERX11923632" alias="SC_EXP_46643_3#26" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923632</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:E2, constructed from sample accession ERS14362530 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TTCCTGGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362530">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362530</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:E2</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="ERX11923627" alias="SC_EXP_46643_3#16" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923627</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:H1, constructed from sample accession ERS14362525 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GGGTGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362525">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362525</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="165" NOMINAL_SDEV="47"/>
        </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="ERX11923645" alias="SC_EXP_46643_3#52" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923645</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:B4, constructed from sample accession ERS14362554 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GTCGGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362554">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362554</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="46"/>
        </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="ERX11923623" alias="SC_EXP_46643_3#8" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923623</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:D1, constructed from sample accession ERS14362522 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CTCATATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362522">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362522</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251665</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="128" NOMINAL_SDEV="24"/>
        </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="ERX11923621" alias="SC_EXP_46643_3#4" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923621</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:B1, constructed from sample accession ERS14362519 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence AGATGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362519">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="123" 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="ERX11923649" alias="SC_EXP_46643_3#60" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923649</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:F4, constructed from sample accession ERS14362557 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GGCGGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362557">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362557</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="44"/>
        </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="ERX11923650" alias="SC_EXP_46643_3#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923650</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:G4, constructed from sample accession ERS14362559 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GTTTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362559">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362559</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="120" NOMINAL_SDEV="18"/>
        </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="ERX11923663" alias="SC_EXP_46643_3#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923663</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:D6, constructed from sample accession ERS14362572 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CAGGCTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362572">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362572</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251715</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="128" NOMINAL_SDEV="24"/>
        </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="ERX11923669" alias="SC_EXP_46643_3#104" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923669</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881797F:D8, constructed from sample accession ERS14362518 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GCTCTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362518">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881797F:D8</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="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="ERX11923643" alias="SC_EXP_46643_3#47" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923643</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:H3, constructed from sample accession ERS14362552 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GCGTACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362552">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362552</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:H3</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="ERX11923652" alias="SC_EXP_46643_3#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923652</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:A5, constructed from sample accession ERS14362561 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CCGGGAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362561">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362561</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="44"/>
        </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="ERX11923622" alias="SC_EXP_46643_3#6" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923622</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:C1, constructed from sample accession ERS14362520 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GTTCGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362520">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362520</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251663</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:C1</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="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="ERX11923642" alias="SC_EXP_46643_3#46" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923642</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:G3, constructed from sample accession ERS14362551 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence AGATCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362551">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362551</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:G3</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="ERX11923644" alias="SC_EXP_46643_3#50" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923644</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:A4, constructed from sample accession ERS14362553 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CCATCTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362553">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362553</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="44"/>
        </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="ERX11923666" alias="SC_EXP_46643_3#101" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923666</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881797F:A8, constructed from sample accession ERS14362512 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GAGGTCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881797F:A8</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="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="ERX11923656" alias="SC_EXP_46643_3#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923656</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:E5, constructed from sample accession ERS14362565 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TGCTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362565">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362565</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="46"/>
        </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="ERX11923640" alias="SC_EXP_46643_3#42" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923640</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:E3, constructed from sample accession ERS14362549 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GCCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362549">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362549</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251692</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:E3</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="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="ERX11923662" alias="SC_EXP_46643_3#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923662</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:C6, constructed from sample accession ERS14362571 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GCCTTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362571">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362571</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251714</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153" 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="ERX11923639" alias="SC_EXP_46643_3#40" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923639</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:D3, constructed from sample accession ERS14362548 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TACGGTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362548">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362548</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251691</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="43"/>
        </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="ERX11923628" alias="SC_EXP_46643_3#17" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923628</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:A2, constructed from sample accession ERS14362526 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GACTATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362526">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362526</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" 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="ERX11923633" alias="SC_EXP_46643_3#28" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923633</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:F2, constructed from sample accession ERS14362531 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GGCTAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362531">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362531</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:F2</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="ERX11923647" alias="SC_EXP_46643_3#56" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923647</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:D4, constructed from sample accession ERS14362556 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TTCAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362556">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362556</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" 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="ERX11923660" alias="SC_EXP_46643_3#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923660</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:A6, constructed from sample accession ERS14362570 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GTTGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362570">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362570</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251713</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="43"/>
        </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="ERX11923655" alias="SC_EXP_46643_3#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923655</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:D5, constructed from sample accession ERS14362564 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GTCGTTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362564">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362564</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251707</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157" NOMINAL_SDEV="43"/>
        </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="ERX11923654" alias="SC_EXP_46643_3#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923654</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:C5, constructed from sample accession ERS14362562 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CGGTATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362562">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362562</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:C5</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="46"/>
        </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="ERX11923620" alias="SC_EXP_46643_3#2" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923620</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:A1, constructed from sample accession ERS14362515 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CAGTTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362515">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362515</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WXS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="113" NOMINAL_SDEV="16"/>
        </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="ERX11923664" alias="SC_EXP_46643_3#99" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923664</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN881797F:G7, constructed from sample accession ERS14362513 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GAGCACGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362513">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251656</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN881797F:G7</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="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="ERX11923641" alias="SC_EXP_46643_3#43" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923641</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:F3, constructed from sample accession ERS14362550 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TGGGTTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362550">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362550</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:F3</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="ERX11923635" alias="SC_EXP_46643_3#32" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923635</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:H2, constructed from sample accession ERS14362533 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence GATTAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362533">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362533</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:H2</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="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="ERX11923629" alias="SC_EXP_46643_3#20" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923629</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:B2, constructed from sample accession ERS14362527 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence CGTCTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362527">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362527</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:B2</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="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="ERX11923631" alias="SC_EXP_46643_3#24" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11923631</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_46643_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP143495">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP143495</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB58437</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN882016R:D2, constructed from sample accession ERS14362529 for study accession ERP143495.  This is part of an Illumina multiplexed sequencing run (46643_3).  This submission includes reads tagged with the sequence TCGGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS14362529">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS14362529</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA112251672</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN882016R:D2</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_SET>
