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      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:A1, constructed from sample accession ERS1474337 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27166918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="502" NOMINAL_SDEV="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#2" accession="ERX2696301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:B1, constructed from sample accession ERS1474338 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27167668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="503" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#3" accession="ERX2696302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:C1, constructed from sample accession ERS1474339 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27168418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="493" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#4" accession="ERX2696303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:D1, constructed from sample accession ERS1474340 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474340">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27169168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="603" NOMINAL_SDEV="197"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#5" accession="ERX2696304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:E1, constructed from sample accession ERS1474341 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27169918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#6" accession="ERX2696305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:F1, constructed from sample accession ERS1474342 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27170668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="548" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#7" accession="ERX2696306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:G1, constructed from sample accession ERS1474343 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27171418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:G1</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="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#8" accession="ERX2696307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:H1, constructed from sample accession ERS1474344 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27172168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:H1</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="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:A2, constructed from sample accession ERS1474345 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474345">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27172918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:A2</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="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#10" accession="ERX2696309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:B2, constructed from sample accession ERS1474346 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27173668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:B2</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="120"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#11" accession="ERX2696310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:C2, constructed from sample accession ERS1474347 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27174418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:C2</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="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21565_1#12" accession="ERX2696311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21565_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21565_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN471598R:D2, constructed from sample accession ERS1474348 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21565_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1474348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1474348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA27175168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN471598R:D2</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="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#1" accession="ERX2696312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:A1, constructed from sample accession ERS1534319 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534319">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72153418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#2" accession="ERX2696313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:B1, constructed from sample accession ERS1534320 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534320">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72154168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:B1</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="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#3" accession="ERX2696314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:C1, constructed from sample accession ERS1534321 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72154918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:C1</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="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#4" accession="ERX2696315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:D1, constructed from sample accession ERS1534322 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72155668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:D1</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="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#5" accession="ERX2696316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:E1, constructed from sample accession ERS1534323 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534323">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72156418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#6" accession="ERX2696317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:F1, constructed from sample accession ERS1534324 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534324">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72157168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:F1</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="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#7" accession="ERX2696318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:G1, constructed from sample accession ERS1534325 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72157918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:G1</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="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#8" accession="ERX2696319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:H1, constructed from sample accession ERS1534326 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534326">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72158668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:H1</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="131"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#9" accession="ERX2696320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:A2, constructed from sample accession ERS1534327 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534327">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72159418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#10" accession="ERX2696321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:B2, constructed from sample accession ERS1534328 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534328">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72160168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:B2</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="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#11" accession="ERX2696322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:C2, constructed from sample accession ERS1534329 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534329">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72160918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:C2</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="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_21897_1#12" accession="ERX2696323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2696323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_21897_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_21897_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq paired end sequencing</TITLE>
    <STUDY_REF accession="ERP016531">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP016531</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB14854</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN475538V:D2, constructed from sample accession ERS1534330 for study accession ERP016531.  This is part of an Illumina multiplexed sequencing run (21897_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1534330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1534330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA72161668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN475538V:D2</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="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Manual Standard WGS (Plate)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
