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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX3361674" alias="SC_EXP_26034_6#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:A1, constructed from sample accession ERS3418186 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418186">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:A1</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361675" alias="SC_EXP_26034_6#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:B1, constructed from sample accession ERS3418204 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AATCGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418204">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418204</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V: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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361676" alias="SC_EXP_26034_6#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:C1, constructed from sample accession ERS3418194 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AATCCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418194">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418194</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="507" NOMINAL_SDEV="121"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361677" alias="SC_EXP_26034_6#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:D1, constructed from sample accession ERS3418188 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418188">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:D1</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="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361678" alias="SC_EXP_26034_6#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:E1, constructed from sample accession ERS3418191 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AAGACGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418191">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:E1</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="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361679" alias="SC_EXP_26034_6#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:F1, constructed from sample accession ERS3418212 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AAGTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:F1</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="118"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361680" alias="SC_EXP_26034_6#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:G1, constructed from sample accession ERS3418229 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AAGTTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:G1</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="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361681" alias="SC_EXP_26034_6#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:H1, constructed from sample accession ERS3418211 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence AAGTTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:H1</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361682" alias="SC_EXP_26034_6#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:A2, constructed from sample accession ERS3418214 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418214">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418214</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:A2</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="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361683" alias="SC_EXP_26034_6#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:B2, constructed from sample accession ERS3418209 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence TTCGCCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418209">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418209</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:B2</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361684" alias="SC_EXP_26034_6#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:C2, constructed from sample accession ERS3418208 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence TGCGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418208">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418208</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:C2</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361685" alias="SC_EXP_26034_6#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:D2, constructed from sample accession ERS3418223 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418223">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:D2</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="119"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361686" alias="SC_EXP_26034_6#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:E2, constructed from sample accession ERS3418202 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence TTATTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418202">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418202</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:E2</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="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361687" alias="SC_EXP_26034_6#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:F2, constructed from sample accession ERS3418201 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence TGACTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418201">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418201</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614015</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V: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="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361688" alias="SC_EXP_26034_6#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:G2, constructed from sample accession ERS3418226 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence GTACAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:G2</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361689" alias="SC_EXP_26034_6#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:H2, constructed from sample accession ERS3418189 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence GGACAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418189">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418189</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="37"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361690" alias="SC_EXP_26034_6#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:A3, constructed from sample accession ERS3418222 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418222">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418222</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:A3</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="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361691" alias="SC_EXP_26034_6#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:B3, constructed from sample accession ERS3418195 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence CTGGCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418195">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:B3</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="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361692" alias="SC_EXP_26034_6#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26034_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26034_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:C3, constructed from sample accession ERS3418199 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26034_6).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418199">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418199</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:C3</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="120"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361693" alias="SC_EXP_26077_2#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:D3, constructed from sample accession ERS3418187 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence TCGGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418187">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="512" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361694" alias="SC_EXP_26077_2#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:E3, constructed from sample accession ERS3418196 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CGCTATTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418196">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418196</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="506" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361695" alias="SC_EXP_26077_2#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:F3, constructed from sample accession ERS3418230 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence AAGACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418230">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418230</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="515" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361696" alias="SC_EXP_26077_2#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:G3, constructed from sample accession ERS3418185 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CAACTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418185">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5613999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="528" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361697" alias="SC_EXP_26077_2#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:H3, constructed from sample accession ERS3418203 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence TTCGAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418203">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418203</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614017</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:H3</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="152"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361698" alias="SC_EXP_26077_2#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:A4, constructed from sample accession ERS3418210 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence GATCAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418210">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418210</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:A4</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="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361699" alias="SC_EXP_26077_2#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:B4, constructed from sample accession ERS3418213 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418213">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418213</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:B4</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="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361700" alias="SC_EXP_26077_2#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:C4, constructed from sample accession ERS3418236 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence TGAGTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="515" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361701" alias="SC_EXP_26077_2#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:D4, constructed from sample accession ERS3418193 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CGAGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418193">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418193</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="533" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361702" alias="SC_EXP_26077_2#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:E4, constructed from sample accession ERS3418231 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="539" NOMINAL_SDEV="151"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361703" alias="SC_EXP_26077_2#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:F4, constructed from sample accession ERS3418184 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CAATGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418184">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5613998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:F4</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="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361704" alias="SC_EXP_26077_2#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:G4, constructed from sample accession ERS3418198 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CATGATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418198">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418198</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614012</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361705" alias="SC_EXP_26077_2#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:H4, constructed from sample accession ERS3418190 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CAGACCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418190">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418190</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="513" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361706" alias="SC_EXP_26077_2#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:A5, constructed from sample accession ERS3418200 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CGAAGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418200">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418200</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614014</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="517" NOMINAL_SDEV="118"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361707" alias="SC_EXP_26077_2#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:B5, constructed from sample accession ERS3418205 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CGTATTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418205">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418205</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361708" alias="SC_EXP_26077_2#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:C5, constructed from sample accession ERS3418228 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence GAATGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361709" alias="SC_EXP_26077_2#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:D5, constructed from sample accession ERS3418206 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418206">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418206</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="522" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361710" alias="SC_EXP_26077_2#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:E5, constructed from sample accession ERS3418197 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_2).  This submission includes reads tagged with the sequence CGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418197">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418197</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:E5</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="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361711" alias="SC_EXP_26077_3#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:F5, constructed from sample accession ERS3418218 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CACAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418218">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418218</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="152"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361712" alias="SC_EXP_26077_3#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:G5, constructed from sample accession ERS3418219 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence TGACTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418219">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418219</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:G5</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="126"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361713" alias="SC_EXP_26077_3#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:H5, constructed from sample accession ERS3418192 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence TTCTGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418192">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418192</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:H5</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="132"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361714" alias="SC_EXP_26077_3#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:A6, constructed from sample accession ERS3418224 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence GATGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418224">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418224</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:A6</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="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361715" alias="SC_EXP_26077_3#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:B6, constructed from sample accession ERS3418238 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418238">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="508" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361716" alias="SC_EXP_26077_3#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:C6, constructed from sample accession ERS3418207 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence GAATATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418207">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418207</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614021</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="448"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361717" alias="SC_EXP_26077_3#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:D6, constructed from sample accession ERS3418237 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence TCGAAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418237">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418237</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:D6</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="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361718" alias="SC_EXP_26077_3#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:E6, constructed from sample accession ERS3418216 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence TCACCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418216">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418216</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:E6</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="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361719" alias="SC_EXP_26077_3#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:F6, constructed from sample accession ERS3418221 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence TGGTCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418221">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418221</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:F6</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="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361720" alias="SC_EXP_26077_3#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:G6, constructed from sample accession ERS3418227 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CAGAAGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418227">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418227</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="303" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361721" alias="SC_EXP_26077_3#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:H6, constructed from sample accession ERS3418215 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CAATCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418215">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418215</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:H6</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="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361722" alias="SC_EXP_26077_3#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:A7, constructed from sample accession ERS3418220 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CTACGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V: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="43"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361723" alias="SC_EXP_26077_3#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:B7, constructed from sample accession ERS3418233 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418233">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418233</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:B7</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="154"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361724" alias="SC_EXP_26077_3#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:C7, constructed from sample accession ERS3418239 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418239">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="566" NOMINAL_SDEV="147"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361725" alias="SC_EXP_26077_3#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:D7, constructed from sample accession ERS3418232 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="544" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361726" alias="SC_EXP_26077_3#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:E7, constructed from sample accession ERS3418235 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361727" alias="SC_EXP_26077_3#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:F7, constructed from sample accession ERS3418217 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence CAACCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418217">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418217</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="542" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361728" alias="SC_EXP_26077_3#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:G7, constructed from sample accession ERS3418234 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence TGAGGCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418234">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418234</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361729" alias="SC_EXP_26077_3#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_26077_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_26077_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN520788V:H7, constructed from sample accession ERS3418225 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (26077_3).  This submission includes reads tagged with the sequence AAGTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3418225">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3418225</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5614039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN520788V:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="22"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361730" alias="SC_EXP_29400_7#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A1, constructed from sample accession ERS3370446 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370446">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361731" alias="SC_EXP_29400_7#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B1, constructed from sample accession ERS3370431 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GTCTACAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568407</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B1</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361732" alias="SC_EXP_29400_7#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C1, constructed from sample accession ERS3370464 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CGCTGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370464">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568441</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C1</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="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361733" alias="SC_EXP_29400_7#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:D1, constructed from sample accession ERS3370434 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GATCAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361734" alias="SC_EXP_29400_7#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:E1, constructed from sample accession ERS3370423 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CGAAGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361735" alias="SC_EXP_29400_7#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:F1, constructed from sample accession ERS3370424 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GATGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568400</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:F1</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="120"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361736" alias="SC_EXP_29400_7#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:G1, constructed from sample accession ERS3370468 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CTACGAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370468">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568445</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361737" alias="SC_EXP_29400_7#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:H1, constructed from sample accession ERS3370427 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GATGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361738" alias="SC_EXP_29400_7#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A2, constructed from sample accession ERS3370422 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568398</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="423" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361739" alias="SC_EXP_29400_7#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B2, constructed from sample accession ERS3370445 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GATTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361740" alias="SC_EXP_29400_7#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C2, constructed from sample accession ERS3370440 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CTACTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361741" alias="SC_EXP_29400_7#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:D2, constructed from sample accession ERS3370442 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GATTCGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361742" alias="SC_EXP_29400_7#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:E2, constructed from sample accession ERS3370472 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence AATCGGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370472">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361743" alias="SC_EXP_29400_7#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:F2, constructed from sample accession ERS3370420 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence TTCGCCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361744" alias="SC_EXP_29400_7#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:G2, constructed from sample accession ERS3370471 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CTGGCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370471">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370471</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361745" alias="SC_EXP_29400_7#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:H2, constructed from sample accession ERS3370421 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAACTTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568397</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361746" alias="SC_EXP_29400_7#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A3, constructed from sample accession ERS3370444 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CGTATTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370444">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568421</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361747" alias="SC_EXP_29400_7#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B3, constructed from sample accession ERS3370433 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361748" alias="SC_EXP_29400_7#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C3, constructed from sample accession ERS3370451 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CTTAATAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361749" alias="SC_EXP_29400_7#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:D3, constructed from sample accession ERS3370449 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAAGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370449">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361750" alias="SC_EXP_29400_7#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:E3, constructed from sample accession ERS3370447 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAAGAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370447">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361751" alias="SC_EXP_29400_7#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:F3, constructed from sample accession ERS3370418 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361752" alias="SC_EXP_29400_7#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:G3, constructed from sample accession ERS3370443 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAATCTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370443">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361753" alias="SC_EXP_29400_7#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:H3, constructed from sample accession ERS3370470 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence CTGATTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370470">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370470</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361754" alias="SC_EXP_29400_7#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A4, constructed from sample accession ERS3370419 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence AATCCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568395</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361755" alias="SC_EXP_29400_7#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B4, constructed from sample accession ERS3370439 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence TGCGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361756" alias="SC_EXP_29400_7#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C4, constructed from sample accession ERS3370463 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAATCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370463">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361757" alias="SC_EXP_29400_7#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:D4, constructed from sample accession ERS3370448 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence TGAGTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370448">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568425</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361758" alias="SC_EXP_29400_7#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:E4, constructed from sample accession ERS3370457 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAATGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361759" alias="SC_EXP_29400_7#30">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_7#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_7#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:F4, constructed from sample accession ERS3370467 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_7).  This submission includes reads tagged with the sequence GAATATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370467">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:F4</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="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361760" alias="SC_EXP_29400_8#1">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:G4, constructed from sample accession ERS3370450 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361761" alias="SC_EXP_29400_8#2">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:H4, constructed from sample accession ERS3370452 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCGGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361762" alias="SC_EXP_29400_8#3">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A5, constructed from sample accession ERS3370425 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence AAGAAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370425">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361763" alias="SC_EXP_29400_8#4">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B5, constructed from sample accession ERS3370462 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370462">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361764" alias="SC_EXP_29400_8#5">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C5, constructed from sample accession ERS3370428 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCGGTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361765" alias="SC_EXP_29400_8#6">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:D5, constructed from sample accession ERS3370475 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCGGTAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370475">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370475</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361766" alias="SC_EXP_29400_8#7">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:E5, constructed from sample accession ERS3370456 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361767" alias="SC_EXP_29400_8#8">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:F5, constructed from sample accession ERS3370469 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370469">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370469</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568446</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361768" alias="SC_EXP_29400_8#9">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:G5, constructed from sample accession ERS3370436 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCGGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361769" alias="SC_EXP_29400_8#10">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:H5, constructed from sample accession ERS3370455 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CGAGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361770" alias="SC_EXP_29400_8#11">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A6, constructed from sample accession ERS3370460 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370460">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361771" alias="SC_EXP_29400_8#12">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B6, constructed from sample accession ERS3370437 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCGAAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="405" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361772" alias="SC_EXP_29400_8#13">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C6, constructed from sample accession ERS3370458 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CTATCATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361773" alias="SC_EXP_29400_8#14">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:D6, constructed from sample accession ERS3370454 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CGCGCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370454">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361774" alias="SC_EXP_29400_8#15">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:E6, constructed from sample accession ERS3370435 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CGAACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361775" alias="SC_EXP_29400_8#16">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:F6, constructed from sample accession ERS3370459 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CTACTGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370459">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361776" alias="SC_EXP_29400_8#17">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:G6, constructed from sample accession ERS3370466 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCTTAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370466">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361777" alias="SC_EXP_29400_8#18">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:H6, constructed from sample accession ERS3370465 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TTAGAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370465">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361778" alias="SC_EXP_29400_8#19">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A7, constructed from sample accession ERS3370426 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence AAGACGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361779" alias="SC_EXP_29400_8#20">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B7, constructed from sample accession ERS3370474 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TTATTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370474">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361780" alias="SC_EXP_29400_8#21">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C7, constructed from sample accession ERS3370453 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CGCTATTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370453">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361781" alias="SC_EXP_29400_8#22">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:D7, constructed from sample accession ERS3370461 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCTATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370461">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370461</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361782" alias="SC_EXP_29400_8#23">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:E7, constructed from sample accession ERS3370441 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370441">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568417</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361783" alias="SC_EXP_29400_8#24">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:F7, constructed from sample accession ERS3370438 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCACCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361784" alias="SC_EXP_29400_8#25">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:G7, constructed from sample accession ERS3370476 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CTGGAAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370476">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370476</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:G7</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="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361785" alias="SC_EXP_29400_8#26">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:H7, constructed from sample accession ERS3370430 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence CGTAAGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361786" alias="SC_EXP_29400_8#27">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:A8, constructed from sample accession ERS3370429 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence AAGAGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361787" alias="SC_EXP_29400_8#28">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:B8, constructed from sample accession ERS3370432 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TCAACGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX3361788" alias="SC_EXP_29400_8#29">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX3361788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_29400_8#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_29400_8#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000190">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000190</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2136</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN547816A:C8, constructed from sample accession ERS3370473 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (29400_8).  This submission includes reads tagged with the sequence TGCGAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS3370473">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS3370473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA5568450</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN547816A:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
