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  <EXPERIMENT accession="ERX4495238" alias="SC_EXP_21765_7#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A1, constructed from sample accession ERS4985334 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495239" alias="SC_EXP_21765_7#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B1, constructed from sample accession ERS4985336 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495240" alias="SC_EXP_21765_7#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:C1, constructed from sample accession ERS4985335 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225350</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="503" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495241" alias="SC_EXP_21765_7#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D1, constructed from sample accession ERS4985333 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="493" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495242" alias="SC_EXP_21765_7#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E1, constructed from sample accession ERS4985340 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495243" alias="SC_EXP_21765_7#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F1, constructed from sample accession ERS4985339 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="489" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495244" alias="SC_EXP_21765_7#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H1, constructed from sample accession ERS4985338 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="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="ERX4495245" alias="SC_EXP_21765_7#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B2, constructed from sample accession ERS4985341 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="494" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495246" alias="SC_EXP_21765_7#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D2, constructed from sample accession ERS4985343 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="489" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495247" alias="SC_EXP_21765_7#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E2, constructed from sample accession ERS4985346 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="509" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495248" alias="SC_EXP_21765_7#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F2, constructed from sample accession ERS4985345 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="509" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495249" alias="SC_EXP_21765_7#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G2, constructed from sample accession ERS4985347 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="509" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495250" alias="SC_EXP_21765_7#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H2, constructed from sample accession ERS4985351 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495251" alias="SC_EXP_21765_7#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A3, constructed from sample accession ERS4985348 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="493" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495252" alias="SC_EXP_21765_7#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B3, constructed from sample accession ERS4985350 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="498" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495253" alias="SC_EXP_21765_7#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:C3, constructed from sample accession ERS4985349 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="514" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495254" alias="SC_EXP_21765_7#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D3, constructed from sample accession ERS4985352 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="505" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495255" alias="SC_EXP_21765_7#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E3, constructed from sample accession ERS4985353 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495256" alias="SC_EXP_21765_7#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F3, constructed from sample accession ERS4985354 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="503" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495257" alias="SC_EXP_21765_7#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G3, constructed from sample accession ERS4985355 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="491" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495258" alias="SC_EXP_21765_7#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H3, constructed from sample accession ERS4985356 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="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="ERX4495259" alias="SC_EXP_21765_7#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D4, constructed from sample accession ERS4985360 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495260" alias="SC_EXP_21765_7#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E4, constructed from sample accession ERS4985361 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="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="ERX4495261" alias="SC_EXP_21765_7#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F4, constructed from sample accession ERS4985362 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="486" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495262" alias="SC_EXP_21765_7#31">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G4, constructed from sample accession ERS4985364 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495263" alias="SC_EXP_21765_7#32">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H4, constructed from sample accession ERS4985363 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="486" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495264" alias="SC_EXP_21765_7#33">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A5, constructed from sample accession ERS4985365 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="485" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495265" alias="SC_EXP_21765_7#34">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B5, constructed from sample accession ERS4985366 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="495" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495266" alias="SC_EXP_21765_7#35">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:C5, constructed from sample accession ERS4985369 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225384</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495267" alias="SC_EXP_21765_7#36">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D5, constructed from sample accession ERS4985367 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="492" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495268" alias="SC_EXP_21765_7#37">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E5, constructed from sample accession ERS4985368 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="502" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495269" alias="SC_EXP_21765_7#38">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F5, constructed from sample accession ERS4985370 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225385</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495270" alias="SC_EXP_21765_7#39">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G5, constructed from sample accession ERS4985371 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225386</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="511" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495271" alias="SC_EXP_21765_7#40">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H5, constructed from sample accession ERS4985372 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225387</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495272" alias="SC_EXP_21765_7#41">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A6, constructed from sample accession ERS4985373 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225388</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495273" alias="SC_EXP_21765_7#42">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B6, constructed from sample accession ERS4985374 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225389</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="488" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495274" alias="SC_EXP_21765_7#43">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:C6, constructed from sample accession ERS4985375 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="498" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495275" alias="SC_EXP_21765_7#44">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D6, constructed from sample accession ERS4985376 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985376">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225391</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495276" alias="SC_EXP_21765_7#45">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E6, constructed from sample accession ERS4985377 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225392</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495277" alias="SC_EXP_21765_7#46">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F6, constructed from sample accession ERS4985378 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495278" alias="SC_EXP_21765_7#47">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G6, constructed from sample accession ERS4985380 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225395</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495279" alias="SC_EXP_21765_7#48">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H6, constructed from sample accession ERS4985379 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985379">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="494" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495280" alias="SC_EXP_21765_7#49">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A7, constructed from sample accession ERS4985381 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="487" NOMINAL_SDEV="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="ERX4495281" alias="SC_EXP_21765_7#50">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B7, constructed from sample accession ERS4985382 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985382">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225397</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495282" alias="SC_EXP_21765_7#51">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:C7, constructed from sample accession ERS4985383 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225398</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="501" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495283" alias="SC_EXP_21765_7#52">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D7, constructed from sample accession ERS4985384 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985384">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495284" alias="SC_EXP_21765_7#53">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E7, constructed from sample accession ERS4985385 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225400</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495285" alias="SC_EXP_21765_7#54">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F7, constructed from sample accession ERS4985386 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495286" alias="SC_EXP_21765_7#55">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G7, constructed from sample accession ERS4985387 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495287" alias="SC_EXP_21765_7#56">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H7, constructed from sample accession ERS4985388 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495288" alias="SC_EXP_21765_7#57">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A8, constructed from sample accession ERS4985389 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="499" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495289" alias="SC_EXP_21765_7#59">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#59</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:C8, constructed from sample accession ERS4985391 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495290" alias="SC_EXP_21765_7#61">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E8, constructed from sample accession ERS4985393 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495291" alias="SC_EXP_21765_7#62">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F8, constructed from sample accession ERS4985394 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495292" alias="SC_EXP_21765_7#64">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H8, constructed from sample accession ERS4985395 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495293" alias="SC_EXP_21765_7#65">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A9, constructed from sample accession ERS4985396 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="490" NOMINAL_SDEV="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="ERX4495294" alias="SC_EXP_21765_7#66">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#66</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B9, constructed from sample accession ERS4985397 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="493" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495295" alias="SC_EXP_21765_7#67">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:C9, constructed from sample accession ERS4985398 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="491" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495296" alias="SC_EXP_21765_7#68">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D9, constructed from sample accession ERS4985399 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="498" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495297" alias="SC_EXP_21765_7#69">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#69</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E9, constructed from sample accession ERS4985400 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495298" alias="SC_EXP_21765_7#70">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#70</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F9, constructed from sample accession ERS4985401 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495299" alias="SC_EXP_21765_7#71">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#71</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G9, constructed from sample accession ERS4985402 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985402">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225417</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495300" alias="SC_EXP_21765_7#72">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#72</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H9, constructed from sample accession ERS4985403 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985403">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495301" alias="SC_EXP_21765_7#73">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A10, constructed from sample accession ERS4985404 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985404">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495302" alias="SC_EXP_21765_7#74">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:B10, constructed from sample accession ERS4985405 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985405">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="481" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495303" alias="SC_EXP_21765_7#76">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:D10, constructed from sample accession ERS4985407 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985407">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="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="ERX4495304" alias="SC_EXP_21765_7#77">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:E10, constructed from sample accession ERS4985408 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495305" alias="SC_EXP_21765_7#78">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#78</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:F10, constructed from sample accession ERS4985409 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495306" alias="SC_EXP_21765_7#79">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:G10, constructed from sample accession ERS4985410 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225425</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495307" alias="SC_EXP_21765_7#80">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:H10, constructed from sample accession ERS4985411 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495308" alias="SC_EXP_21765_7#81">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#81</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470753G:A11, constructed from sample accession ERS4985412 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470753G:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495309" alias="SC_EXP_21765_7#82">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#82</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A1, constructed from sample accession ERS4985413 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495310" alias="SC_EXP_21765_7#83">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#83</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B1, constructed from sample accession ERS4985414 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495311" alias="SC_EXP_21765_7#84">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#84</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C1, constructed from sample accession ERS4985415 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495312" alias="SC_EXP_21765_7#86">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:E1, constructed from sample accession ERS4985417 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495313" alias="SC_EXP_21765_7#87">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F1, constructed from sample accession ERS4985419 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495314" alias="SC_EXP_21765_7#88">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G1, constructed from sample accession ERS4985418 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="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="ERX4495315" alias="SC_EXP_21765_7#90">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#90</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A2, constructed from sample accession ERS4985420 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495316" alias="SC_EXP_21765_7#91">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B2, constructed from sample accession ERS4985421 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495317" alias="SC_EXP_21765_7#92">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C2, constructed from sample accession ERS4985422 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495318" alias="SC_EXP_21765_7#93">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#93</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D2, constructed from sample accession ERS4985423 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495319" alias="SC_EXP_21765_7#94">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#94</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:E2, constructed from sample accession ERS4985424 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="488" NOMINAL_SDEV="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="ERX4495320" alias="SC_EXP_21765_7#96">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#96</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G2, constructed from sample accession ERS4985425 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="485" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495321" alias="SC_EXP_21765_7#98">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#98</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A3, constructed from sample accession ERS4985426 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225441</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495322" alias="SC_EXP_21765_7#99">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#99</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B3, constructed from sample accession ERS4985427 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495323" alias="SC_EXP_21765_7#100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#100</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C3, constructed from sample accession ERS4985428 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495324" alias="SC_EXP_21765_7#101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#101</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D3, constructed from sample accession ERS4985429 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="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="ERX4495325" alias="SC_EXP_21765_7#103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#103</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F3, constructed from sample accession ERS4985431 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225446</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495326" alias="SC_EXP_21765_7#104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#104</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G3, constructed from sample accession ERS4985432 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495327" alias="SC_EXP_21765_7#105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#105</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:H3, constructed from sample accession ERS4985433 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495328" alias="SC_EXP_21765_7#106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#106</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A4, constructed from sample accession ERS4985434 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495329" alias="SC_EXP_21765_7#108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#108</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C4, constructed from sample accession ERS4985436 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495330" alias="SC_EXP_21765_7#109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#109</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D4, constructed from sample accession ERS4985437 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="494" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495331" alias="SC_EXP_21765_7#110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#110</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:E4, constructed from sample accession ERS4985438 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495332" alias="SC_EXP_21765_7#111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#111</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F4, constructed from sample accession ERS4985439 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495333" alias="SC_EXP_21765_7#112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#112</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G4, constructed from sample accession ERS4985440 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495334" alias="SC_EXP_21765_7#113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#113</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:H4, constructed from sample accession ERS4985441 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985441">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495335" alias="SC_EXP_21765_7#114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#114</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A5, constructed from sample accession ERS4985442 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495336" alias="SC_EXP_21765_7#115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#115</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B5, constructed from sample accession ERS4985443 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985443">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495337" alias="SC_EXP_21765_7#117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#117</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D5, constructed from sample accession ERS4985445 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495338" alias="SC_EXP_21765_7#119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#119</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F5, constructed from sample accession ERS4985447 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985447">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495339" alias="SC_EXP_21765_7#120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#120</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G5, constructed from sample accession ERS4985448 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985448">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495340" alias="SC_EXP_21765_7#121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#121</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:H5, constructed from sample accession ERS4985449 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985449">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495341" alias="SC_EXP_21765_7#122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#122</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A6, constructed from sample accession ERS4985450 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495342" alias="SC_EXP_21765_7#123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#123</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B6, constructed from sample accession ERS4985451 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495343" alias="SC_EXP_21765_7#124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#124</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C6, constructed from sample accession ERS4985452 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495344" alias="SC_EXP_21765_7#125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#125</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D6, constructed from sample accession ERS4985458 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495345" alias="SC_EXP_21765_7#126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#126</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:E6, constructed from sample accession ERS4985460 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985460">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495346" alias="SC_EXP_21765_7#127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#127</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F6, constructed from sample accession ERS4985459 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985459">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495347" alias="SC_EXP_21765_7#128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#128</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G6, constructed from sample accession ERS4985461 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985461">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985461</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495348" alias="SC_EXP_21765_7#129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#129</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:H6, constructed from sample accession ERS4985462 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985462">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495349" alias="SC_EXP_21765_7#130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#130</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A7, constructed from sample accession ERS4985463 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985463">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495350" alias="SC_EXP_21765_7#132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#132</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C7, constructed from sample accession ERS4985465 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985465">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495351" alias="SC_EXP_21765_7#133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#133</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D7, constructed from sample accession ERS4985468 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985468">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495352" alias="SC_EXP_21765_7#134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#134</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:E7, constructed from sample accession ERS4985466 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985466">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495353" alias="SC_EXP_21765_7#135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#135</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F7, constructed from sample accession ERS4985467 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985467">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495354" alias="SC_EXP_21765_7#136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#136</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G7, constructed from sample accession ERS4985469 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985469">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495355" alias="SC_EXP_21765_7#137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#137</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:H7, constructed from sample accession ERS4985470 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985470">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985470</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495356" alias="SC_EXP_21765_7#138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#138</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A8, constructed from sample accession ERS4985471 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985471">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985471</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495357" alias="SC_EXP_21765_7#139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#139</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B8, constructed from sample accession ERS4985472 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985472">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495358" alias="SC_EXP_21765_7#140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#140</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C8, constructed from sample accession ERS4985473 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985473">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495359" alias="SC_EXP_21765_7#141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#141</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D8, constructed from sample accession ERS4985475 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985475">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985475</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="71"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495360" alias="SC_EXP_21765_7#143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#143</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F8, constructed from sample accession ERS4985474 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985474">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495361" alias="SC_EXP_21765_7#144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#144</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G8, constructed from sample accession ERS4985476 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985476">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985476</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495362" alias="SC_EXP_21765_7#147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#147</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B9, constructed from sample accession ERS4985479 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985479">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985479</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495363" alias="SC_EXP_21765_7#148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#148</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C9, constructed from sample accession ERS4985480 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985480">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985480</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495364" alias="SC_EXP_21765_7#149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#149</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D9, constructed from sample accession ERS4985481 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985481">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985481</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225496</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495365" alias="SC_EXP_21765_7#150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#150</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:E9, constructed from sample accession ERS4985482 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985482">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985482</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225497</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495366" alias="SC_EXP_21765_7#151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#151</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:F9, constructed from sample accession ERS4985483 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985483">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985483</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225498</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495367" alias="SC_EXP_21765_7#152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#152</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G9, constructed from sample accession ERS4985484 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985484">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985484</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225499</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495368" alias="SC_EXP_21765_7#153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#153</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:H9, constructed from sample accession ERS4985485 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985485">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985485</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225500</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495369" alias="SC_EXP_21765_7#154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#154</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:A10, constructed from sample accession ERS4985486 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985486">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985486</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225501</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495370" alias="SC_EXP_21765_7#155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#155</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:B10, constructed from sample accession ERS4985487 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985487">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985487</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225502</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="459" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495371" alias="SC_EXP_21765_7#156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#156</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:C10, constructed from sample accession ERS4985489 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985489">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985489</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225504</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="69"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495372" alias="SC_EXP_21765_7#157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#157</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:D10, constructed from sample accession ERS4985488 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985488">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985488</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225503</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495373" alias="SC_EXP_21765_7#158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#158</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:E10, constructed from sample accession ERS4985490 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985490">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985490</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225505</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495374" alias="SC_EXP_21765_7#160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#160</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:G10, constructed from sample accession ERS4985492 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985492">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985492</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225507</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495375" alias="SC_EXP_21765_7#161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#161</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470754H:H10, constructed from sample accession ERS4985493 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985493">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225508</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470754H:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495376" alias="SC_EXP_21765_7#163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#163</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A1, constructed from sample accession ERS4985495 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985495">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985495</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225510</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495377" alias="SC_EXP_21765_7#164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#164</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B1, constructed from sample accession ERS4985496 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985496">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985496</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225511</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495378" alias="SC_EXP_21765_7#165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#165</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:C1, constructed from sample accession ERS4985497 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985497">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985497</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="485" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495379" alias="SC_EXP_21765_7#166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#166</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D1, constructed from sample accession ERS4985453 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985453">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495380" alias="SC_EXP_21765_7#168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#168</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F1, constructed from sample accession ERS4985456 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="487" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495381" alias="SC_EXP_21765_7#170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#170</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H1, constructed from sample accession ERS4985457 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495382" alias="SC_EXP_21765_7#171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#171</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A2, constructed from sample accession ERS4985498 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985498">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985498</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495383" alias="SC_EXP_21765_7#173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#173</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:C2, constructed from sample accession ERS4985500 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985500">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985500</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495384" alias="SC_EXP_21765_7#174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#174</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D2, constructed from sample accession ERS4985501 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985501">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985501</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225516</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="485" NOMINAL_SDEV="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="ERX4495385" alias="SC_EXP_21765_7#175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#175</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:E2, constructed from sample accession ERS4985502 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985502">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985502</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225517</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="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="ERX4495386" alias="SC_EXP_21765_7#176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#176</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F2, constructed from sample accession ERS4985503 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985503">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985503</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495387" alias="SC_EXP_21765_7#178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#178</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H2, constructed from sample accession ERS4985505 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985505">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985505</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495388" alias="SC_EXP_21765_7#179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#179</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A3, constructed from sample accession ERS4985506 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985506">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985506</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495389" alias="SC_EXP_21765_7#180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#180</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B3, constructed from sample accession ERS4985507 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985507">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985507</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495390" alias="SC_EXP_21765_7#181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#181</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:C3, constructed from sample accession ERS4985509 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985509">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985509</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="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="ERX4495391" alias="SC_EXP_21765_7#182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#182</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D3, constructed from sample accession ERS4985508 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985508">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985508</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495392" alias="SC_EXP_21765_7#184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#184</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F3, constructed from sample accession ERS4985510 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985510">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985510</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495393" alias="SC_EXP_21765_7#185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#185</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:G3, constructed from sample accession ERS4985513 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985513">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="476" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495394" alias="SC_EXP_21765_7#186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#186</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H3, constructed from sample accession ERS4985512 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495395" alias="SC_EXP_21765_7#187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#187</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A4, constructed from sample accession ERS4985515 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985515">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985515</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495396" alias="SC_EXP_21765_7#188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#188</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B4, constructed from sample accession ERS4985514 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985514">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="493" NOMINAL_SDEV="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="ERX4495397" alias="SC_EXP_21765_7#190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#190</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D4, constructed from sample accession ERS4985518 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985518">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985518</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495398" alias="SC_EXP_21765_7#191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#191</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:E4, constructed from sample accession ERS4985517 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985517">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985517</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495399" alias="SC_EXP_21765_7#192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#192</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F4, constructed from sample accession ERS4985519 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985519">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985519</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495400" alias="SC_EXP_21765_7#194">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#194</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H4, constructed from sample accession ERS4985520 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985520">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985520</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495401" alias="SC_EXP_21765_7#195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#195</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A5, constructed from sample accession ERS4985522 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985522">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985522</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225537</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495402" alias="SC_EXP_21765_7#196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#196</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B5, constructed from sample accession ERS4985521 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985521">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985521</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="475" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495403" alias="SC_EXP_21765_7#197">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#197</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:C5, constructed from sample accession ERS4985523 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985523">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985523</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225538</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495404" alias="SC_EXP_21765_7#198">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#198</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D5, constructed from sample accession ERS4985524 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985524">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985524</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225539</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="504" 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="ERX4495405" alias="SC_EXP_21765_7#199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#199</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:E5, constructed from sample accession ERS4985526 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985526">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985526</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225541</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="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="ERX4495406" alias="SC_EXP_21765_7#200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#200</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F5, constructed from sample accession ERS4985525 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985525">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985525</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225540</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495407" alias="SC_EXP_21765_7#201">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#201</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:G5, constructed from sample accession ERS4985527 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985527">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985527</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225542</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="471" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495408" alias="SC_EXP_21765_7#203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#203</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A6, constructed from sample accession ERS4985529 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985529">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985529</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225544</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495409" alias="SC_EXP_21765_7#204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#204</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B6, constructed from sample accession ERS4985530 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985530">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985530</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225545</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495410" alias="SC_EXP_21765_7#206">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#206</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D6, constructed from sample accession ERS4985533 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985533">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985533</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225548</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495411" alias="SC_EXP_21765_7#208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#208</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F6, constructed from sample accession ERS4985534 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985534">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985534</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225549</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="452" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495412" alias="SC_EXP_21765_7#209">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#209</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:G6, constructed from sample accession ERS4985538 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985538">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985538</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495413" alias="SC_EXP_21765_7#210">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#210</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H6, constructed from sample accession ERS4985535 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985535">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985535</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225550</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495414" alias="SC_EXP_21765_7#211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#211</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A7, constructed from sample accession ERS4985536 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985536">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985536</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225551</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="474" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495415" alias="SC_EXP_21765_7#212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#212</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B7, constructed from sample accession ERS4985537 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985537">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985537</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225552</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="488" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495416" alias="SC_EXP_21765_7#214">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#214</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D7, constructed from sample accession ERS4985540 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985540">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985540</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225555</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495417" alias="SC_EXP_21765_7#215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#215</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:E7, constructed from sample accession ERS4985541 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985541">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985541</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225556</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="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="ERX4495418" alias="SC_EXP_21765_7#216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#216</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F7, constructed from sample accession ERS4985542 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985542">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985542</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225557</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495419" alias="SC_EXP_21765_7#217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#217</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:G7, constructed from sample accession ERS4985544 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985544">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985544</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225559</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="441" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495420" alias="SC_EXP_21765_7#218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#218</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H7, constructed from sample accession ERS4985543 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985543">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985543</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225558</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="459" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495421" alias="SC_EXP_21765_7#219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#219</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A8, constructed from sample accession ERS4985546 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985546">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985546</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225561</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="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="ERX4495422" alias="SC_EXP_21765_7#220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#220</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B8, constructed from sample accession ERS4985545 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985545">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985545</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225560</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="491" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495423" alias="SC_EXP_21765_7#221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#221</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:C8, constructed from sample accession ERS4985549 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985549">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985549</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225564</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495424" alias="SC_EXP_21765_7#223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#223</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:E8, constructed from sample accession ERS4985548 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985548">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985548</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225563</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="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="ERX4495425" alias="SC_EXP_21765_7#224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#224</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F8, constructed from sample accession ERS4985550 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985550">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985550</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225565</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495426" alias="SC_EXP_21765_7#225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#225</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:G8, constructed from sample accession ERS4985552 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985552">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985552</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="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="ERX4495427" alias="SC_EXP_21765_7#227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#227</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A9, constructed from sample accession ERS4985554 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985554">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985554</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495428" alias="SC_EXP_21765_7#228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#228</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B9, constructed from sample accession ERS4985553 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985553">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985553</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="482" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495429" alias="SC_EXP_21765_7#230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#230</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D9, constructed from sample accession ERS4985556 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985556">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985556</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495430" alias="SC_EXP_21765_7#232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#232</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F9, constructed from sample accession ERS4985557 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985557">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985557</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225572</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495431" alias="SC_EXP_21765_7#233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#233</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:G9, constructed from sample accession ERS4985559 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985559">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985559</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225574</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495432" alias="SC_EXP_21765_7#234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#234</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H9, constructed from sample accession ERS4985560 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985560">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985560</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225575</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495433" alias="SC_EXP_21765_7#235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#235</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A10, constructed from sample accession ERS4985561 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985561">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985561</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225576</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="483" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495434" alias="SC_EXP_21765_7#236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#236</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:B10, constructed from sample accession ERS4985562 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985562">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985562</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225577</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="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="ERX4495435" alias="SC_EXP_21765_7#237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#237</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:C10, constructed from sample accession ERS4985564 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985564">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985564</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225579</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495436" alias="SC_EXP_21765_7#238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#238</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:D10, constructed from sample accession ERS4985563 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985563">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985563</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225578</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495437" alias="SC_EXP_21765_7#239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#239</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:E10, constructed from sample accession ERS4985565 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985565">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985565</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225580</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495438" alias="SC_EXP_21765_7#240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#240</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:F10, constructed from sample accession ERS4985566 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985566">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985566</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225581</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495439" alias="SC_EXP_21765_7#241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#241</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:G10, constructed from sample accession ERS4985568 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985568">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985568</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225583</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495440" alias="SC_EXP_21765_7#242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#242</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#242</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:H10, constructed from sample accession ERS4985567 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTCGCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985567">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985567</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225582</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495441" alias="SC_EXP_21765_7#243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#243</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#243</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470828I:A11, constructed from sample accession ERS4985569 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985569">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985569</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225584</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470828I:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495442" alias="SC_EXP_21765_7#244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#244</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#244</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A1, constructed from sample accession ERS4985570 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985570">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985570</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495443" alias="SC_EXP_21765_7#245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#245</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B1, constructed from sample accession ERS4985571 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985571">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985571</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225586</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495444" alias="SC_EXP_21765_7#246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#246</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C1, constructed from sample accession ERS4985572 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985572">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985572</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225587</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495445" alias="SC_EXP_21765_7#247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#247</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D1, constructed from sample accession ERS4985573 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985573">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985573</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495446" alias="SC_EXP_21765_7#248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#248</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:E1, constructed from sample accession ERS4985574 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985574">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985574</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495447" alias="SC_EXP_21765_7#250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#250</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G1, constructed from sample accession ERS4985575 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985575">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985575</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495448" alias="SC_EXP_21765_7#251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#251</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:H1, constructed from sample accession ERS4985576 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985576">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985576</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495449" alias="SC_EXP_21765_7#252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#252</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A2, constructed from sample accession ERS4985577 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985577">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985577</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495450" alias="SC_EXP_21765_7#254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#254</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C2, constructed from sample accession ERS4985579 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985579">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985579</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495451" alias="SC_EXP_21765_7#255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#255</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D2, constructed from sample accession ERS4985580 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985580">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985580</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495452" alias="SC_EXP_21765_7#257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#257</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:F2, constructed from sample accession ERS4985581 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985581">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985581</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="445" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495453" alias="SC_EXP_21765_7#258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#258</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G2, constructed from sample accession ERS4985582 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985582">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985582</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="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="ERX4495454" alias="SC_EXP_21765_7#259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#259</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:H2, constructed from sample accession ERS4985583 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985583">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985583</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="480" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495455" alias="SC_EXP_21765_7#260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#260</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A3, constructed from sample accession ERS4985584 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985584">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985584</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495456" alias="SC_EXP_21765_7#261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#261</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B3, constructed from sample accession ERS4985586 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985586">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985586</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495457" alias="SC_EXP_21765_7#262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#262</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#262</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C3, constructed from sample accession ERS4985585 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985585">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985585</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="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="ERX4495458" alias="SC_EXP_21765_7#263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#263</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#263</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D3, constructed from sample accession ERS4985588 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985588">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985588</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="500" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495459" alias="SC_EXP_21765_7#264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#264</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#264</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:E3, constructed from sample accession ERS4985587 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985587">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985587</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495460" alias="SC_EXP_21765_7#266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#266</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#266</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G3, constructed from sample accession ERS4985590 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985590">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985590</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="470" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495461" alias="SC_EXP_21765_7#268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#268</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#268</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A4, constructed from sample accession ERS4985591 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985591">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985591</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225606</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495462" alias="SC_EXP_21765_7#269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495462</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#269</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B4, constructed from sample accession ERS4985593 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985593">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985593</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495463" alias="SC_EXP_21765_7#270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#270</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#270</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C4, constructed from sample accession ERS4985596 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985596">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985596</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495464" alias="SC_EXP_21765_7#271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495464</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#271</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#271</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D4, constructed from sample accession ERS4985595 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985595">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985595</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225610</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495465" alias="SC_EXP_21765_7#273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495465</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#273</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:F4, constructed from sample accession ERS4985597 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985597">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985597</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225612</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495466" alias="SC_EXP_21765_7#274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#274</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#274</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G4, constructed from sample accession ERS4985598 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985598">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985598</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495467" alias="SC_EXP_21765_7#275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#275</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#275</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:H4, constructed from sample accession ERS4985599 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985599">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985599</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225614</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495468" alias="SC_EXP_21765_7#278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#278</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#278</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C5, constructed from sample accession ERS4985602 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985602">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985602</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225617</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495469" alias="SC_EXP_21765_7#279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#279</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#279</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D5, constructed from sample accession ERS4985603 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985603">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985603</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225618</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="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="ERX4495470" alias="SC_EXP_21765_7#280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#280</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#280</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:E5, constructed from sample accession ERS4985604 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985604">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985604</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225619</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495471" alias="SC_EXP_21765_7#281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#281</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:F5, constructed from sample accession ERS4985605 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985605">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985605</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495472" alias="SC_EXP_21765_7#282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#282</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#282</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G5, constructed from sample accession ERS4985606 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985606">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985606</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225621</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495473" alias="SC_EXP_21765_7#283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#283</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#283</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:H5, constructed from sample accession ERS4985608 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985608">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985608</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495474" alias="SC_EXP_21765_7#284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#284</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#284</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A6, constructed from sample accession ERS4985607 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985607">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985607</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225622</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495475" alias="SC_EXP_21765_7#285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#285</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B6, constructed from sample accession ERS4985609 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985609">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985609</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225624</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495476" alias="SC_EXP_21765_7#287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#287</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#287</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D6, constructed from sample accession ERS4985611 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985611">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985611</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495477" alias="SC_EXP_21765_7#288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#288</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#288</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:E6, constructed from sample accession ERS4985612 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985612">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985612</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="472" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495478" alias="SC_EXP_21765_7#290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#290</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#290</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G6, constructed from sample accession ERS4985614 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985614">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985614</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="75"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495479" alias="SC_EXP_21765_7#293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#293</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B7, constructed from sample accession ERS4985618 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985618">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985618</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495480" alias="SC_EXP_21765_7#294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#294</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C7, constructed from sample accession ERS4985617 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985617">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985617</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495481" alias="SC_EXP_21765_7#295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#295</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D7, constructed from sample accession ERS4985619 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985619">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985619</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="461" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495482" alias="SC_EXP_21765_7#296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#296</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:E7, constructed from sample accession ERS4985620 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985620">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985620</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495483" alias="SC_EXP_21765_7#298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G7, constructed from sample accession ERS4985621 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985621">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985621</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495484" alias="SC_EXP_21765_7#299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:H7, constructed from sample accession ERS4985623 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985623">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985623</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495485" alias="SC_EXP_21765_7#300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A8, constructed from sample accession ERS4985624 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985624">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985624</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495486" alias="SC_EXP_21765_7#301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B8, constructed from sample accession ERS4985626 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985626">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985626</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495487" alias="SC_EXP_21765_7#302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C8, constructed from sample accession ERS4985625 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985625">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985625</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495488" alias="SC_EXP_21765_7#304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#304</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:E8, constructed from sample accession ERS4985627 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985627">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985627</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495489" alias="SC_EXP_21765_7#305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#305</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:F8, constructed from sample accession ERS4985630 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985630">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985630</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495490" alias="SC_EXP_21765_7#307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#307</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:H8, constructed from sample accession ERS4985629 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985629">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985629</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495491" alias="SC_EXP_21765_7#308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A9, constructed from sample accession ERS4985631 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985631">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985631</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495492" alias="SC_EXP_21765_7#309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B9, constructed from sample accession ERS4985632 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985632">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="449" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495493" alias="SC_EXP_21765_7#310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:C9, constructed from sample accession ERS4985633 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985633">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225648</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495494" alias="SC_EXP_21765_7#311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D9, constructed from sample accession ERS4985636 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985636">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225651</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495495" alias="SC_EXP_21765_7#312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:E9, constructed from sample accession ERS4985634 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985634">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225649</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="466" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495496" alias="SC_EXP_21765_7#313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:F9, constructed from sample accession ERS4985635 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985635">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985635</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225650</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="444" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495497" alias="SC_EXP_21765_7#315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#315</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:H9, constructed from sample accession ERS4985637 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GACGGATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985637">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225652</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="464" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495498" alias="SC_EXP_21765_7#316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#316</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A10, constructed from sample accession ERS4985639 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985639">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985639</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225654</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495499" alias="SC_EXP_21765_7#317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#317</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B10, constructed from sample accession ERS4985640 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985640">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985640</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495500" alias="SC_EXP_21765_7#319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:D10, constructed from sample accession ERS4985642 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985642">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985642</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225657</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495501" alias="SC_EXP_21765_7#321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:F10, constructed from sample accession ERS4985644 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985644">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985644</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495502" alias="SC_EXP_21765_7#322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:G10, constructed from sample accession ERS4985645 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985645">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985645</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="465" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495503" alias="SC_EXP_21765_7#324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#324</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:A11, constructed from sample accession ERS4985646 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985646">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX4495504" alias="SC_EXP_21765_7#325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX4495504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21765_7#325</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21765_7#325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP017250">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP017250</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB15489</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN470829J:B11, constructed from sample accession ERS4985647 for study accession ERP017250.  This is part of an Illumina multiplexed sequencing run (21765_7).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS4985647">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS4985647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7225662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN470829J:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="86"/>
        </LIBRARY_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>
