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      <PRIMARY_ID>ERX4442728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B2, constructed from sample accession ERS3525219 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_1).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="341" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442729" alias="SC_EXP_30555_1#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H2, constructed from sample accession ERS3525225 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_1).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="ERX4442730" alias="SC_EXP_30555_1#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G4, constructed from sample accession ERS3525240 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_1).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442731" alias="SC_EXP_30555_1#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D5, constructed from sample accession ERS3525245 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_1).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442732" alias="SC_EXP_30555_1#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H6, constructed from sample accession ERS3525257 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_1).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="328" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442733" alias="SC_EXP_30555_1#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G8, constructed from sample accession ERS3525272 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_1).  This submission includes reads tagged with the sequence AAGACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="342" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="ERX4442734" alias="SC_EXP_30555_2#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B2, constructed from sample accession ERS3525219 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_2).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="338" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442735" alias="SC_EXP_30555_2#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H2, constructed from sample accession ERS3525225 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_2).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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      <PRIMARY_ID>ERX4442736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G4, constructed from sample accession ERS3525240 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_2).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442737" alias="SC_EXP_30555_2#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D5, constructed from sample accession ERS3525245 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_2).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442738" alias="SC_EXP_30555_2#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H6, constructed from sample accession ERS3525257 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_2).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="329" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442739" alias="SC_EXP_30555_2#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G8, constructed from sample accession ERS3525272 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_2).  This submission includes reads tagged with the sequence AAGACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442740" alias="SC_EXP_30555_3#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B2, constructed from sample accession ERS3525219 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_3).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442741" alias="SC_EXP_30555_3#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H2, constructed from sample accession ERS3525225 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_3).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="341" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442742" alias="SC_EXP_30555_3#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G4, constructed from sample accession ERS3525240 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_3).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442743" alias="SC_EXP_30555_3#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D5, constructed from sample accession ERS3525245 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_3).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442744" alias="SC_EXP_30555_3#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H6, constructed from sample accession ERS3525257 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_3).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="329" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442745" alias="SC_EXP_30555_3#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G8, constructed from sample accession ERS3525272 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_3).  This submission includes reads tagged with the sequence AAGACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442746" alias="SC_EXP_30555_4#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F3, constructed from sample accession ERS3525231 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_4).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="329" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442747" alias="SC_EXP_30555_4#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H3, constructed from sample accession ERS3525233 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_4).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="337" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442748" alias="SC_EXP_30555_4#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A7, constructed from sample accession ERS3525258 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_4).  This submission includes reads tagged with the sequence AAGACGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="341" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442749" alias="SC_EXP_30555_4#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G7, constructed from sample accession ERS3525264 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_4).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="335" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442750" alias="SC_EXP_30555_4#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A8, constructed from sample accession ERS3525266 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_4).  This submission includes reads tagged with the sequence AAGAGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="334" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442751" alias="SC_EXP_30555_5#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F3, constructed from sample accession ERS3525231 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_5).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="325" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442752" alias="SC_EXP_30555_5#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H3, constructed from sample accession ERS3525233 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_5).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="329" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442753" alias="SC_EXP_30555_5#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A7, constructed from sample accession ERS3525258 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_5).  This submission includes reads tagged with the sequence AAGACGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442754" alias="SC_EXP_30555_5#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G7, constructed from sample accession ERS3525264 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_5).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="328" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442755" alias="SC_EXP_30555_5#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A8, constructed from sample accession ERS3525266 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_5).  This submission includes reads tagged with the sequence AAGAGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="327" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442756" alias="SC_EXP_30555_6#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F3, constructed from sample accession ERS3525231 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_6).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="330" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442757" alias="SC_EXP_30555_6#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H3, constructed from sample accession ERS3525233 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_6).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442758" alias="SC_EXP_30555_6#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A7, constructed from sample accession ERS3525258 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_6).  This submission includes reads tagged with the sequence AAGACGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="338" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442759" alias="SC_EXP_30555_6#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G7, constructed from sample accession ERS3525264 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_6).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="336" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442760" alias="SC_EXP_30555_6#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A8, constructed from sample accession ERS3525266 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_6).  This submission includes reads tagged with the sequence AAGAGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="332" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442761" alias="SC_EXP_30555_7#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F3, constructed from sample accession ERS3525231 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_7).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="324" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442762" alias="SC_EXP_30555_7#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H3, constructed from sample accession ERS3525233 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_7).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="329" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442763" alias="SC_EXP_30555_7#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A7, constructed from sample accession ERS3525258 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_7).  This submission includes reads tagged with the sequence AAGACGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442764" alias="SC_EXP_30555_7#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G7, constructed from sample accession ERS3525264 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_7).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="328" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442765" alias="SC_EXP_30555_7#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A8, constructed from sample accession ERS3525266 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_7).  This submission includes reads tagged with the sequence AAGAGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="328" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442766" alias="SC_EXP_30555_8#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F3, constructed from sample accession ERS3525231 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_8).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="327" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442767" alias="SC_EXP_30555_8#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H3, constructed from sample accession ERS3525233 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_8).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="328" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442768" alias="SC_EXP_30555_8#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A7, constructed from sample accession ERS3525258 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_8).  This submission includes reads tagged with the sequence AAGACGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442769" alias="SC_EXP_30555_8#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G7, constructed from sample accession ERS3525264 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_8).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="329" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442770" alias="SC_EXP_30555_8#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30555_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30555_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A8, constructed from sample accession ERS3525266 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30555_8).  This submission includes reads tagged with the sequence AAGAGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="331" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442771" alias="SC_EXP_30595_1#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C1, constructed from sample accession ERS3525212 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_1).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="351" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442772" alias="SC_EXP_30595_1#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D2, constructed from sample accession ERS3525221 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_1).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442773" alias="SC_EXP_30595_1#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B5, constructed from sample accession ERS3525243 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_1).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="339" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442774" alias="SC_EXP_30595_1#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C6, constructed from sample accession ERS3525252 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_1).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442775" alias="SC_EXP_30595_1#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F6, constructed from sample accession ERS3525255 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_1).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442776" alias="SC_EXP_30595_1#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D7, constructed from sample accession ERS3525261 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_1).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442777" alias="SC_EXP_30595_2#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C1, constructed from sample accession ERS3525212 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_2).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="361" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442778" alias="SC_EXP_30595_2#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D2, constructed from sample accession ERS3525221 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_2).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="352" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442779" alias="SC_EXP_30595_2#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B5, constructed from sample accession ERS3525243 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_2).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442780" alias="SC_EXP_30595_2#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C6, constructed from sample accession ERS3525252 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_2).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442781" alias="SC_EXP_30595_2#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F6, constructed from sample accession ERS3525255 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_2).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="354" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442782" alias="SC_EXP_30595_2#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D7, constructed from sample accession ERS3525261 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_2).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442783" alias="SC_EXP_30595_3#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C1, constructed from sample accession ERS3525212 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_3).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="356" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442784" alias="SC_EXP_30595_3#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D2, constructed from sample accession ERS3525221 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_3).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442785" alias="SC_EXP_30595_3#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B5, constructed from sample accession ERS3525243 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_3).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442786" alias="SC_EXP_30595_3#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C6, constructed from sample accession ERS3525252 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_3).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442787" alias="SC_EXP_30595_3#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F6, constructed from sample accession ERS3525255 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_3).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442788" alias="SC_EXP_30595_3#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D7, constructed from sample accession ERS3525261 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_3).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="342" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442789" alias="SC_EXP_30595_4#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C1, constructed from sample accession ERS3525212 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_4).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="355" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442790" alias="SC_EXP_30595_4#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D2, constructed from sample accession ERS3525221 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_4).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442791" alias="SC_EXP_30595_4#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B5, constructed from sample accession ERS3525243 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_4).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442792" alias="SC_EXP_30595_4#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C6, constructed from sample accession ERS3525252 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_4).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442793" alias="SC_EXP_30595_4#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F6, constructed from sample accession ERS3525255 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_4).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442794" alias="SC_EXP_30595_4#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D7, constructed from sample accession ERS3525261 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_4).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="342" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442795" alias="SC_EXP_30595_5#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C1, constructed from sample accession ERS3525212 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_5).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="356" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442796" alias="SC_EXP_30595_5#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D2, constructed from sample accession ERS3525221 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_5).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442797" alias="SC_EXP_30595_5#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B5, constructed from sample accession ERS3525243 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_5).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442798" alias="SC_EXP_30595_5#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C6, constructed from sample accession ERS3525252 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_5).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442799" alias="SC_EXP_30595_5#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F6, constructed from sample accession ERS3525255 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_5).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442800" alias="SC_EXP_30595_5#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D7, constructed from sample accession ERS3525261 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_5).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442801" alias="SC_EXP_30595_6#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B2, constructed from sample accession ERS3525219 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_6).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442802" alias="SC_EXP_30595_6#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H2, constructed from sample accession ERS3525225 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_6).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442803" alias="SC_EXP_30595_6#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G4, constructed from sample accession ERS3525240 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_6).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442804" alias="SC_EXP_30595_6#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D5, constructed from sample accession ERS3525245 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_6).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442805" alias="SC_EXP_30595_6#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H6, constructed from sample accession ERS3525257 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_6).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442806" alias="SC_EXP_30595_6#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G8, constructed from sample accession ERS3525272 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_6).  This submission includes reads tagged with the sequence AAGACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442807" alias="SC_EXP_30595_7#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B2, constructed from sample accession ERS3525219 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_7).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442808" alias="SC_EXP_30595_7#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H2, constructed from sample accession ERS3525225 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_7).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442809" alias="SC_EXP_30595_7#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G4, constructed from sample accession ERS3525240 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_7).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442810" alias="SC_EXP_30595_7#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D5, constructed from sample accession ERS3525245 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_7).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442811" alias="SC_EXP_30595_7#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H6, constructed from sample accession ERS3525257 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_7).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442812" alias="SC_EXP_30595_7#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G8, constructed from sample accession ERS3525272 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_7).  This submission includes reads tagged with the sequence AAGACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442813" alias="SC_EXP_30595_8#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B2, constructed from sample accession ERS3525219 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_8).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="337" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442814" alias="SC_EXP_30595_8#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H2, constructed from sample accession ERS3525225 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_8).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="337" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442815" alias="SC_EXP_30595_8#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G4, constructed from sample accession ERS3525240 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_8).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525240">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525240</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="342" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442816" alias="SC_EXP_30595_8#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D5, constructed from sample accession ERS3525245 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_8).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="337" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442817" alias="SC_EXP_30595_8#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:H6, constructed from sample accession ERS3525257 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_8).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="327" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442818" alias="SC_EXP_30595_8#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30595_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30595_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:G8, constructed from sample accession ERS3525272 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30595_8).  This submission includes reads tagged with the sequence AAGACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="339" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442819" alias="SC_EXP_30597_2#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442819</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B1, constructed from sample accession ERS3525211 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_2).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442820" alias="SC_EXP_30597_2#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442820</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A2, constructed from sample accession ERS3525218 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_2).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442821" alias="SC_EXP_30597_2#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442821</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C3, constructed from sample accession ERS3525228 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_2).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442822" alias="SC_EXP_30597_2#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442822</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C4, constructed from sample accession ERS3525236 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_2).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442823" alias="SC_EXP_30597_2#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442823</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F5, constructed from sample accession ERS3525247 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_2).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="352" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442824" alias="SC_EXP_30597_2#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442824</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:E8, constructed from sample accession ERS3525270 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_2).  This submission includes reads tagged with the sequence AAGTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442825" alias="SC_EXP_30597_3#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442825</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B1, constructed from sample accession ERS3525211 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_3).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442826" alias="SC_EXP_30597_3#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442826</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A2, constructed from sample accession ERS3525218 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_3).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442827" alias="SC_EXP_30597_3#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C3, constructed from sample accession ERS3525228 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_3).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442828" alias="SC_EXP_30597_3#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442828</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C4, constructed from sample accession ERS3525236 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_3).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="341" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442829" alias="SC_EXP_30597_3#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F5, constructed from sample accession ERS3525247 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_3).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="353" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442830" alias="SC_EXP_30597_3#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442830</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:E8, constructed from sample accession ERS3525270 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_3).  This submission includes reads tagged with the sequence AAGTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442831" alias="SC_EXP_30597_4#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442831</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B1, constructed from sample accession ERS3525211 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_4).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442832" alias="SC_EXP_30597_4#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442832</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A2, constructed from sample accession ERS3525218 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_4).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442833" alias="SC_EXP_30597_4#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442833</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C3, constructed from sample accession ERS3525228 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_4).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442834" alias="SC_EXP_30597_4#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442834</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C4, constructed from sample accession ERS3525236 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_4).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442835" alias="SC_EXP_30597_4#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442835</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F5, constructed from sample accession ERS3525247 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_4).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442836" alias="SC_EXP_30597_4#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442836</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:E8, constructed from sample accession ERS3525270 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_4).  This submission includes reads tagged with the sequence AAGTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442837" alias="SC_EXP_30597_5#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442837</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B1, constructed from sample accession ERS3525211 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_5).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442838" alias="SC_EXP_30597_5#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442838</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A2, constructed from sample accession ERS3525218 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_5).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442839" alias="SC_EXP_30597_5#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442839</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C3, constructed from sample accession ERS3525228 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_5).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442840" alias="SC_EXP_30597_5#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442840</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C4, constructed from sample accession ERS3525236 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_5).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="339" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442841" alias="SC_EXP_30597_5#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442841</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F5, constructed from sample accession ERS3525247 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_5).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442842" alias="SC_EXP_30597_5#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442842</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:E8, constructed from sample accession ERS3525270 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_5).  This submission includes reads tagged with the sequence AAGTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442843" alias="SC_EXP_30597_6#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B1, constructed from sample accession ERS3525211 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_6).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442844" alias="SC_EXP_30597_6#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442844</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A2, constructed from sample accession ERS3525218 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_6).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442845" alias="SC_EXP_30597_6#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442845</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C3, constructed from sample accession ERS3525228 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_6).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="341" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442846" alias="SC_EXP_30597_6#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442846</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C4, constructed from sample accession ERS3525236 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_6).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="341" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442847" alias="SC_EXP_30597_6#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F5, constructed from sample accession ERS3525247 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_6).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442848" alias="SC_EXP_30597_6#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442848</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:E8, constructed from sample accession ERS3525270 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_6).  This submission includes reads tagged with the sequence AAGTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442849" alias="SC_EXP_30597_7#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442849</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B1, constructed from sample accession ERS3525211 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_7).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442850" alias="SC_EXP_30597_7#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442850</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:A2, constructed from sample accession ERS3525218 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_7).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442851" alias="SC_EXP_30597_7#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442851</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C3, constructed from sample accession ERS3525228 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_7).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442852" alias="SC_EXP_30597_7#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442852</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C4, constructed from sample accession ERS3525236 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_7).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="341" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442853" alias="SC_EXP_30597_7#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442853</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F5, constructed from sample accession ERS3525247 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_7).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="352" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442854" alias="SC_EXP_30597_7#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442854</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:E8, constructed from sample accession ERS3525270 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_7).  This submission includes reads tagged with the sequence AAGTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525270">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442855" alias="SC_EXP_30597_8#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C1, constructed from sample accession ERS3525212 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_8).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="356" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442856" alias="SC_EXP_30597_8#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D2, constructed from sample accession ERS3525221 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_8).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442857" alias="SC_EXP_30597_8#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:B5, constructed from sample accession ERS3525243 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_8).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442858" alias="SC_EXP_30597_8#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:C6, constructed from sample accession ERS3525252 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_8).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442859" alias="SC_EXP_30597_8#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:F6, constructed from sample accession ERS3525255 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_8).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="352" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4442860" alias="SC_EXP_30597_8#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4442860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_30597_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_30597_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP115837">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP115837</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB33075</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547973M:D7, constructed from sample accession ERS3525261 for study accession ERP115837.  This is part of an Illumina multiplexed sequencing run (30597_8).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3525261">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3525261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5721641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547973M:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
