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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX11282855" alias="SC_EXP_47423_1#114" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282855</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I14, constructed from sample accession ERS13472961 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282396" alias="SC_EXP_47408_1#272" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282396</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#272</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J8, constructed from sample accession ERS13473132 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282717" alias="SC_EXP_47408_1#807" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282717</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#807</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I24, constructed from sample accession ERS13472905 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282308" alias="SC_EXP_47408_1#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282308</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K8, constructed from sample accession ERS13472768 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472768">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282733" alias="SC_EXP_47408_1#918" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282733</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#918</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L4, constructed from sample accession ERS13473118 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282322" alias="SC_EXP_47408_1#104" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282322</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G12, constructed from sample accession ERS13472782 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472782">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282357" alias="SC_EXP_47408_1#139" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282357</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C22, constructed from sample accession ERS13472895 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282920" alias="SC_EXP_47423_1#179" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282920</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F7, constructed from sample accession ERS13472800 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472800">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472800</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282775" alias="SC_EXP_47408_1#960" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282775</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#960</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L16, constructed from sample accession ERS13473030 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282590" alias="SC_EXP_47408_1#620" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282590</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#620</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F14, constructed from sample accession ERS13473020 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473020">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473020</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282503" alias="SC_EXP_47408_1#439" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282503</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#439</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C14, constructed from sample accession ERS13472787 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472787">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282345" alias="SC_EXP_47408_1#127" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282345</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E18, constructed from sample accession ERS13472884 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282542" alias="SC_EXP_47408_1#478" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282542</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#478</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I24, constructed from sample accession ERS13472905 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282883" alias="SC_EXP_47423_1#142" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282883</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I22, constructed from sample accession ERS13472989 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282893" alias="SC_EXP_47423_1#152" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282893</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O24, constructed from sample accession ERS15395412 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282428" alias="SC_EXP_47408_1#304" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282428</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D18, constructed from sample accession ERS13473034 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473034">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282475" alias="SC_EXP_47408_1#411" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282475</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#411</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K6, constructed from sample accession ERS13472762 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472762">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472762</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282457" alias="SC_EXP_47408_1#393" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282457</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#393</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G2, constructed from sample accession ERS13472866 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282509" alias="SC_EXP_47408_1#445" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282509</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#445</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O14, constructed from sample accession ERS13472794 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472794">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282838" alias="SC_EXP_47423_1#97" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282838</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G10, constructed from sample accession ERS13472942 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282300" alias="SC_EXP_47408_1#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282300</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K6, constructed from sample accession ERS13472762 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472762">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472762</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282383" alias="SC_EXP_47408_1#259" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282383</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L4, constructed from sample accession ERS13473118 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282287" alias="SC_EXP_47408_1#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282287</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A4, constructed from sample accession ERS13472870 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282904" alias="SC_EXP_47423_1#163" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282904</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F3, constructed from sample accession ERS13472740 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472740">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472740</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282336" alias="SC_EXP_47408_1#118" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282336</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C16, constructed from sample accession ERS13472795 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472795">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472795</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282691" alias="SC_EXP_47408_1#781" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282691</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#781</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M16, constructed from sample accession ERS13472880 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472880">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282823" alias="SC_EXP_47423_1#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282823</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I6, constructed from sample accession ERS13472927 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472927">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472927</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282723" alias="SC_EXP_47408_1#908" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282723</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#908</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F2, constructed from sample accession ERS13473108 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282353" alias="SC_EXP_47408_1#135" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282353</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I20, constructed from sample accession ERS13472892 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282942" alias="SC_EXP_47423_1#201" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282942</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F13, constructed from sample accession ERS13472822 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472822">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472822</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282624" alias="SC_EXP_47408_1#654" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282624</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H24, constructed from sample accession ERS13473054 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473054">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282805" alias="SC_EXP_47423_1#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282805</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C2, constructed from sample accession ERS13472911 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282485" alias="SC_EXP_47408_1#421" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282485</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#421</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O8, constructed from sample accession ERS13472770 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472770">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472770</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282421" alias="SC_EXP_47408_1#297" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282421</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D16, constructed from sample accession ERS13473027 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282533" alias="SC_EXP_47408_1#469" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282533</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#469</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E22, constructed from sample accession ERS13472897 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472897">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282395" alias="SC_EXP_47408_1#271" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282395</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#271</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H8, constructed from sample accession ERS13473131 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282687" alias="SC_EXP_47408_1#777" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282687</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#777</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E16, constructed from sample accession ERS13472876 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472876">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282427" alias="SC_EXP_47408_1#303" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282427</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B18, constructed from sample accession ERS13473033 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282759" alias="SC_EXP_47408_1#944" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282759</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#944</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H12, constructed from sample accession ERS13473014 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282925" alias="SC_EXP_47423_1#184" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282925</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:P7, constructed from sample accession ERS13472805 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472805">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:P7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282721" alias="SC_EXP_47408_1#906" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282721</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#906</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B2, constructed from sample accession ERS13473112 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282538" alias="SC_EXP_47408_1#474" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282538</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#474</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A24, constructed from sample accession ERS13472900 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472900">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282582" alias="SC_EXP_47408_1#612" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282582</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#612</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D12, constructed from sample accession ERS13473016 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282748" alias="SC_EXP_47408_1#933" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282748</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#933</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N8, constructed from sample accession ERS13473135 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282419" alias="SC_EXP_47408_1#295" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282419</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N14, constructed from sample accession ERS13473026 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473026">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282728" alias="SC_EXP_47408_1#913" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282728</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#913</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B4, constructed from sample accession ERS13473115 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282754" alias="SC_EXP_47408_1#939" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282754</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#939</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L10, constructed from sample accession ERS13473010 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282310" alias="SC_EXP_47408_1#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282310</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O8, constructed from sample accession ERS13472770 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472770">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472770</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282561" alias="SC_EXP_47408_1#591" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282561</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#591</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D6, constructed from sample accession ERS13473122 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282463" alias="SC_EXP_47408_1#399" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282463</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#399</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C4, constructed from sample accession ERS13472871 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472871">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282630" alias="SC_EXP_47408_1#720" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282630</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#720</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C2, constructed from sample accession ERS13472864 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472864">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282597" alias="SC_EXP_47408_1#627" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282597</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#627</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F16, constructed from sample accession ERS13473032 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282550" alias="SC_EXP_47408_1#580" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282550</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#580</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J2, constructed from sample accession ERS13473111 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282584" alias="SC_EXP_47408_1#614" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282584</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#614</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H12, constructed from sample accession ERS13473014 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282702" alias="SC_EXP_47408_1#792" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282702</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#792</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G20, constructed from sample accession ERS13472891 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282508" alias="SC_EXP_47408_1#444" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282508</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#444</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M14, constructed from sample accession ERS13472803 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472803">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472803</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282665" alias="SC_EXP_47408_1#755" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282665</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#755</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I10, constructed from sample accession ERS13472774 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472774">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282330" alias="SC_EXP_47408_1#112" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282330</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G14, constructed from sample accession ERS13472789 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472789">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282881" alias="SC_EXP_47423_1#140" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282881</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E22, constructed from sample accession ERS13472984 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282718" alias="SC_EXP_47408_1#808" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282718</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#808</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K24, constructed from sample accession ERS13472907 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472907">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472907</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282311" alias="SC_EXP_47408_1#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282311</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A10, constructed from sample accession ERS13472771 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472771">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282675" alias="SC_EXP_47408_1#765" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282675</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#765</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M12, constructed from sample accession ERS13472785 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472785">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282794" alias="SC_EXP_47408_1#979" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282794</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#979</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J22, constructed from sample accession ERS13473050 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473050">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282462" alias="SC_EXP_47408_1#398" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282462</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#398</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A4, constructed from sample accession ERS13472870 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282320" alias="SC_EXP_47408_1#102" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282320</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C12, constructed from sample accession ERS13472779 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472779">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282456" alias="SC_EXP_47408_1#392" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282456</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#392</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E2, constructed from sample accession ERS13472865 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472865">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472865</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282325" alias="SC_EXP_47408_1#107" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282325</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M12, constructed from sample accession ERS13472785 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472785">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282849" alias="SC_EXP_47423_1#108" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282849</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M12, constructed from sample accession ERS13472954 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282940" alias="SC_EXP_47423_1#199" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282940</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B13, constructed from sample accession ERS13472825 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472825">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282868" alias="SC_EXP_47423_1#127" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282868</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C18, constructed from sample accession ERS13472973 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472973">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282417" alias="SC_EXP_47408_1#293" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282417</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J14, constructed from sample accession ERS13473023 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473023">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282730" alias="SC_EXP_47408_1#915" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282730</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#915</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F4, constructed from sample accession ERS13473119 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282412" alias="SC_EXP_47408_1#288" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282412</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#288</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N12, constructed from sample accession ERS13473018 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282521" alias="SC_EXP_47408_1#457" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282521</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#457</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G18, constructed from sample accession ERS13472885 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282292" alias="SC_EXP_47408_1#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282292</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K4, constructed from sample accession ERS13472752 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472752">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472752</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282664" alias="SC_EXP_47408_1#754" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282664</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#754</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G10, constructed from sample accession ERS13472773 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472773">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472773</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282472" alias="SC_EXP_47408_1#408" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282472</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#408</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E6, constructed from sample accession ERS13472757 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472757">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282294" alias="SC_EXP_47408_1#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282294</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O4, constructed from sample accession ERS13472751 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472751">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282488" alias="SC_EXP_47408_1#424" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282488</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#424</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E10, constructed from sample accession ERS13472772 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472772">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472772</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282344" alias="SC_EXP_47408_1#126" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282344</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C18, constructed from sample accession ERS13472883 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472883">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472883</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282845" alias="SC_EXP_47423_1#104" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282845</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E12, constructed from sample accession ERS13472950 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282788" alias="SC_EXP_47408_1#973" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282788</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#973</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J20, constructed from sample accession ERS13473044 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473044">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282806" alias="SC_EXP_47423_1#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282806</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G2, constructed from sample accession ERS13472910 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472910">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282449" alias="SC_EXP_47408_1#325" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282449</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#325</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H24, constructed from sample accession ERS13473054 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473054">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282375" alias="SC_EXP_47408_1#251" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282375</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J2, constructed from sample accession ERS13473111 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282333" alias="SC_EXP_47408_1#115" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282333</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M14, constructed from sample accession ERS13472803 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472803">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472803</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282622" alias="SC_EXP_47408_1#652" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282622</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D24, constructed from sample accession ERS13473051 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473051">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282931" alias="SC_EXP_47423_1#190" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282931</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L9, constructed from sample accession ERS13472812 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472812">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472812</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282961" alias="SC_EXP_47423_1#220" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282961</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B19, constructed from sample accession ERS13472841 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472841">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282309" alias="SC_EXP_47408_1#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282309</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M8, constructed from sample accession ERS13472769 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472769">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472769</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282438" alias="SC_EXP_47408_1#314" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282438</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J20, constructed from sample accession ERS13473044 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473044">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282827" alias="SC_EXP_47423_1#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282827</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A8, constructed from sample accession ERS13472929 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472929">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282880" alias="SC_EXP_47423_1#139" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282880</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C22, constructed from sample accession ERS13472987 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282647" alias="SC_EXP_47408_1#737" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282647</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#737</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E6, constructed from sample accession ERS13472757 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472757">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282672" alias="SC_EXP_47408_1#762" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282672</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#762</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G12, constructed from sample accession ERS13472782 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472782">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282793" alias="SC_EXP_47408_1#978" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282793</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#978</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H22, constructed from sample accession ERS13473049 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282917" alias="SC_EXP_47423_1#176" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282917</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:P5, constructed from sample accession ERS13472797 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472797">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:P5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282467" alias="SC_EXP_47408_1#403" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282467</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#403</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K4, constructed from sample accession ERS13472752 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472752">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472752</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282830" alias="SC_EXP_47423_1#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282830</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G8, constructed from sample accession ERS13472932 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472932">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472932</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282715" alias="SC_EXP_47408_1#805" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282715</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#805</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E24, constructed from sample accession ERS13472906 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472906">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472906</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282906" alias="SC_EXP_47423_1#165" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282906</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J3, constructed from sample accession ERS13472742 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472742">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472742</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282863" alias="SC_EXP_47423_1#122" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282863</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I16, constructed from sample accession ERS13472967 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282352" alias="SC_EXP_47408_1#134" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282352</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G20, constructed from sample accession ERS13472891 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282918" alias="SC_EXP_47423_1#177" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282918</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B7, constructed from sample accession ERS13472798 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472798">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282374" alias="SC_EXP_47408_1#250" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282374</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H2, constructed from sample accession ERS13473110 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282818" alias="SC_EXP_47423_1#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282818</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O4, constructed from sample accession ERS13472933 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472933">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282975" alias="SC_EXP_47423_1#234" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282975</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B23, constructed from sample accession ERS13472856 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472856">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472856</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282866" alias="SC_EXP_47423_1#125" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282866</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O16, constructed from sample accession ERS13472971 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282861" alias="SC_EXP_47423_1#120" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282861</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E16, constructed from sample accession ERS13472969 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282751" alias="SC_EXP_47408_1#936" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282751</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#936</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F10, constructed from sample accession ERS13473006 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282803" alias="SC_EXP_47408_1#988" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282803</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#988</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:P24, constructed from sample accession ERS15395416 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:P24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282757" alias="SC_EXP_47408_1#942" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282757</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#942</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D12, constructed from sample accession ERS13473016 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282372" alias="SC_EXP_47408_1#248" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282372</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D2, constructed from sample accession ERS13473109 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282574" alias="SC_EXP_47408_1#604" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282574</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#604</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B10, constructed from sample accession ERS13473136 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282424" alias="SC_EXP_47408_1#300" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282424</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J16, constructed from sample accession ERS13473029 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282410" alias="SC_EXP_47408_1#286" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282410</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#286</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J12, constructed from sample accession ERS13473015 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282841" alias="SC_EXP_47423_1#100" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282841</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M10, constructed from sample accession ERS13472945 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282514" alias="SC_EXP_47408_1#450" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282514</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#450</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I16, constructed from sample accession ERS13472878 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472878">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282783" alias="SC_EXP_47408_1#968" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282783</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#968</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N18, constructed from sample accession ERS13473039 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282735" alias="SC_EXP_47408_1#920" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282735</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#920</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B6, constructed from sample accession ERS13473121 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282795" alias="SC_EXP_47408_1#980" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282795</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#980</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L22, constructed from sample accession ERS13473056 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282924" alias="SC_EXP_47423_1#183" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282924</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N7, constructed from sample accession ERS13472806 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472806">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472806</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282825" alias="SC_EXP_47423_1#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282825</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M6, constructed from sample accession ERS13472930 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472930">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472930</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282546" alias="SC_EXP_47408_1#576" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282546</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#576</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B2, constructed from sample accession ERS13473112 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282347" alias="SC_EXP_47408_1#129" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282347</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I18, constructed from sample accession ERS13472886 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282452" alias="SC_EXP_47408_1#328" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282452</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#328</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N24, constructed from sample accession ERS15395415 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282977" alias="SC_EXP_47423_1#236" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282977</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F23, constructed from sample accession ERS13472857 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282870" alias="SC_EXP_47423_1#129" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282870</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G18, constructed from sample accession ERS13472975 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282513" alias="SC_EXP_47408_1#449" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282513</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#449</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G16, constructed from sample accession ERS13472877 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472877">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282453" alias="SC_EXP_47408_1#329" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282453</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#329</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:P24, constructed from sample accession ERS15395416 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:P24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282407" alias="SC_EXP_47408_1#283" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282407</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#283</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D12, constructed from sample accession ERS13473016 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282459" alias="SC_EXP_47408_1#395" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282459</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#395</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K2, constructed from sample accession ERS13472867 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472867">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282644" alias="SC_EXP_47408_1#734" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282644</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#734</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O4, constructed from sample accession ERS13472751 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472751">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282797" alias="SC_EXP_47408_1#982" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282797</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#982</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D24, constructed from sample accession ERS13473051 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473051">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282779" alias="SC_EXP_47408_1#964" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282779</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#964</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F18, constructed from sample accession ERS13473035 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473035">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282434" alias="SC_EXP_47408_1#310" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282434</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B20, constructed from sample accession ERS13473040 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473040">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282567" alias="SC_EXP_47408_1#597" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282567</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#597</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B8, constructed from sample accession ERS13473129 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282764" alias="SC_EXP_47408_1#949" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282764</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#949</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D14, constructed from sample accession ERS13473021 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282625" alias="SC_EXP_47408_1#655" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282625</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J24, constructed from sample accession ERS13473055 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282714" alias="SC_EXP_47408_1#804" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282714</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#804</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C24, constructed from sample accession ERS13472901 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472901">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282295" alias="SC_EXP_47408_1#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282295</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A6, constructed from sample accession ERS13472754 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472754">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282907" alias="SC_EXP_47423_1#166" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282907</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L3, constructed from sample accession ERS13472745 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472745">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282366" alias="SC_EXP_47408_1#148" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282366</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G24, constructed from sample accession ERS13472903 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472903">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282939" alias="SC_EXP_47423_1#198" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282939</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N11, constructed from sample accession ERS13472820 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472820">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472820</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282451" alias="SC_EXP_47408_1#327" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282451</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#327</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L24, constructed from sample accession ERS13473057 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282874" alias="SC_EXP_47423_1#133" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282874</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E20, constructed from sample accession ERS13472979 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472979">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282446" alias="SC_EXP_47408_1#322" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282446</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B24, constructed from sample accession ERS13473052 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282399" alias="SC_EXP_47408_1#275" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282399</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#275</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B10, constructed from sample accession ERS13473136 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282560" alias="SC_EXP_47408_1#590" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282560</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#590</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B6, constructed from sample accession ERS13473121 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282943" alias="SC_EXP_47423_1#202" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282943</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#202</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H13, constructed from sample accession ERS13472823 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472823">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472823</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282535" alias="SC_EXP_47408_1#471" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282535</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#471</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I22, constructed from sample accession ERS13472898 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472898">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282611" alias="SC_EXP_47408_1#641" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282611</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#641</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F20, constructed from sample accession ERS13473042 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282476" alias="SC_EXP_47408_1#412" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282476</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#412</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M6, constructed from sample accession ERS13472761 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472761">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472761</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282524" alias="SC_EXP_47408_1#460" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282524</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#460</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M18, constructed from sample accession ERS13472888 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282875" alias="SC_EXP_47423_1#134" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282875</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G20, constructed from sample accession ERS13472980 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282729" alias="SC_EXP_47408_1#914" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282729</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#914</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D4, constructed from sample accession ERS13473116 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282481" alias="SC_EXP_47408_1#417" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282481</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#417</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G8, constructed from sample accession ERS13472765 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472765">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282902" alias="SC_EXP_47423_1#161" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282902</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B3, constructed from sample accession ERS13472738 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472738">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472738</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282365" alias="SC_EXP_47408_1#147" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282365</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E24, constructed from sample accession ERS13472906 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472906">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472906</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282307" alias="SC_EXP_47408_1#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282307</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I8, constructed from sample accession ERS13472767 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472767">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472767</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282919" alias="SC_EXP_47423_1#178" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282919</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D7, constructed from sample accession ERS13472799 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472799">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282778" alias="SC_EXP_47408_1#963" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282778</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#963</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D18, constructed from sample accession ERS13473034 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473034">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282836" alias="SC_EXP_47423_1#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282836</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C10, constructed from sample accession ERS13472939 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472939">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282911" alias="SC_EXP_47423_1#170" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282911</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D5, constructed from sample accession ERS13472755 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472755">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472755</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375768</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282640" alias="SC_EXP_47408_1#730" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282640</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#730</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G4, constructed from sample accession ERS13472874 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472874">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282293" alias="SC_EXP_47408_1#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282293</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M4, constructed from sample accession ERS13472753 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472753">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472753</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282548" alias="SC_EXP_47408_1#578" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282548</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#578</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F2, constructed from sample accession ERS13473108 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282746" alias="SC_EXP_47408_1#931" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282746</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#931</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J8, constructed from sample accession ERS13473132 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282299" alias="SC_EXP_47408_1#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282299</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I6, constructed from sample accession ERS13472759 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472759">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472759</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282331" alias="SC_EXP_47408_1#113" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282331</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I14, constructed from sample accession ERS13472790 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472790">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282573" alias="SC_EXP_47408_1#603" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282573</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#603</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N8, constructed from sample accession ERS13473135 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282777" alias="SC_EXP_47408_1#962" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282777</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#962</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B18, constructed from sample accession ERS13473033 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282510" alias="SC_EXP_47408_1#446" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282510</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#446</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A16, constructed from sample accession ERS13472793 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472793">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282771" alias="SC_EXP_47408_1#956" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282771</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#956</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D16, constructed from sample accession ERS13473027 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282684" alias="SC_EXP_47408_1#774" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282684</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#774</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O14, constructed from sample accession ERS13472794 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472794">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282340" alias="SC_EXP_47408_1#122" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282340</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K16, constructed from sample accession ERS13472879 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472879">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282564" alias="SC_EXP_47408_1#594" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282564</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#594</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J6, constructed from sample accession ERS13473125 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282726" alias="SC_EXP_47408_1#911" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282726</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#911</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L2, constructed from sample accession ERS13473113 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282605" alias="SC_EXP_47408_1#635" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282605</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#635</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H18, constructed from sample accession ERS13473036 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282377" alias="SC_EXP_47408_1#253" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282377</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N2, constructed from sample accession ERS13473114 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282588" alias="SC_EXP_47408_1#618" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282588</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#618</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B14, constructed from sample accession ERS13473019 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473019">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282504" alias="SC_EXP_47408_1#440" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282504</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#440</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E14, constructed from sample accession ERS13472792 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472792">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472792</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282515" alias="SC_EXP_47408_1#451" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282515</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#451</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K16, constructed from sample accession ERS13472879 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472879">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282382" alias="SC_EXP_47408_1#258" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282382</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J4, constructed from sample accession ERS13473123 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282738" alias="SC_EXP_47408_1#923" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282738</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#923</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H6, constructed from sample accession ERS13473124 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282782" alias="SC_EXP_47408_1#967" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282782</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#967</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L18, constructed from sample accession ERS13473038 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473038">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282962" alias="SC_EXP_47423_1#221" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282962</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D19, constructed from sample accession ERS13472843 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472843">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282753" alias="SC_EXP_47408_1#938" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282753</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#938</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J10, constructed from sample accession ERS13473009 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473009">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282970" alias="SC_EXP_47423_1#229" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282970</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F21, constructed from sample accession ERS13472851 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282306" alias="SC_EXP_47408_1#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282306</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G8, constructed from sample accession ERS13472765 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472765">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282928" alias="SC_EXP_47423_1#187" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282928</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F9, constructed from sample accession ERS13472809 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472809">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472809</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282470" alias="SC_EXP_47408_1#406" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282470</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#406</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A6, constructed from sample accession ERS13472754 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472754">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282913" alias="SC_EXP_47423_1#172" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282913</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H5, constructed from sample accession ERS13472747 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472747">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472747</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282285" alias="SC_EXP_47408_1#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282285</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M2, constructed from sample accession ERS13472872 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472872">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282741" alias="SC_EXP_47408_1#926" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282741</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#926</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N6, constructed from sample accession ERS13473128 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282454" alias="SC_EXP_47408_1#390" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282454</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#390</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A2, constructed from sample accession ERS13472863 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282505" alias="SC_EXP_47408_1#441" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282505</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#441</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G14, constructed from sample accession ERS13472789 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472789">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282885" alias="SC_EXP_47423_1#144" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282885</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M22, constructed from sample accession ERS13472990 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472990">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282934" alias="SC_EXP_47423_1#193" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282934</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#193</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D11, constructed from sample accession ERS13472815 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472815">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472815</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282857" alias="SC_EXP_47423_1#116" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282857</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M14, constructed from sample accession ERS13472964 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282912" alias="SC_EXP_47423_1#171" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282912</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F5, constructed from sample accession ERS13472749 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472749">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472749</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282767" alias="SC_EXP_47408_1#952" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282767</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#952</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J14, constructed from sample accession ERS13473023 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473023">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282518" alias="SC_EXP_47408_1#454" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282518</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#454</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A18, constructed from sample accession ERS13472882 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472882">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472882</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282388" alias="SC_EXP_47408_1#264" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282388</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#264</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H6, constructed from sample accession ERS13473124 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282342" alias="SC_EXP_47408_1#124" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282342</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O16, constructed from sample accession ERS13472881 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472881">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472881</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282570" alias="SC_EXP_47408_1#600" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282570</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#600</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H8, constructed from sample accession ERS13473131 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282425" alias="SC_EXP_47408_1#301" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282425</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L16, constructed from sample accession ERS13473030 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282742" alias="SC_EXP_47408_1#927" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282742</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#927</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B8, constructed from sample accession ERS13473129 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282798" alias="SC_EXP_47408_1#983" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282798</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#983</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F24, constructed from sample accession ERS13473053 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282465" alias="SC_EXP_47408_1#401" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282465</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#401</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G4, constructed from sample accession ERS13472874 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472874">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282339" alias="SC_EXP_47408_1#121" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282339</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I16, constructed from sample accession ERS13472878 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472878">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282387" alias="SC_EXP_47408_1#263" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282387</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#263</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F6, constructed from sample accession ERS13473127 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282541" alias="SC_EXP_47408_1#477" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282541</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#477</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G24, constructed from sample accession ERS13472903 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472903">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282471" alias="SC_EXP_47408_1#407" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282471</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#407</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C6, constructed from sample accession ERS13472756 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472756">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472756</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282929" alias="SC_EXP_47423_1#188" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282929</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H9, constructed from sample accession ERS13472810 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472810">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472810</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282596" alias="SC_EXP_47408_1#626" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282596</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#626</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D16, constructed from sample accession ERS13473027 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282642" alias="SC_EXP_47408_1#732" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282642</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#732</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K4, constructed from sample accession ERS13472752 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472752">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472752</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282367" alias="SC_EXP_47408_1#149" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282367</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I24, constructed from sample accession ERS13472905 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282802" alias="SC_EXP_47408_1#987" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282802</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#987</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N24, constructed from sample accession ERS15395415 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282969" alias="SC_EXP_47423_1#228" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282969</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D21, constructed from sample accession ERS13472850 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472850">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472850</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282786" alias="SC_EXP_47408_1#971" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282786</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#971</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F20, constructed from sample accession ERS13473042 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282556" alias="SC_EXP_47408_1#586" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282556</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#586</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H4, constructed from sample accession ERS13473117 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282808" alias="SC_EXP_47423_1#67" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282808</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K2, constructed from sample accession ERS13472913 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472913">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282692" alias="SC_EXP_47408_1#782" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282692</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#782</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O16, constructed from sample accession ERS13472881 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472881">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472881</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282668" alias="SC_EXP_47408_1#758" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282668</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#758</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O10, constructed from sample accession ERS13472778 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472778">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282575" alias="SC_EXP_47408_1#605" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282575</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#605</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D10, constructed from sample accession ERS13473137 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282583" alias="SC_EXP_47408_1#613" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282583</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#613</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F12, constructed from sample accession ERS13473013 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473013">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282693" alias="SC_EXP_47408_1#783" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282693</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#783</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A18, constructed from sample accession ERS13472882 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472882">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472882</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282790" alias="SC_EXP_47408_1#975" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282790</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#975</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B22, constructed from sample accession ERS13473046 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282620" alias="SC_EXP_47408_1#650" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282620</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#650</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L22, constructed from sample accession ERS13473056 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282469" alias="SC_EXP_47408_1#405" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282469</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#405</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O4, constructed from sample accession ERS13472751 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472751">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282474" alias="SC_EXP_47408_1#410" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282474</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#410</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I6, constructed from sample accession ERS13472759 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472759">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472759</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282839" alias="SC_EXP_47423_1#98" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282839</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I10, constructed from sample accession ERS13472943 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282526" alias="SC_EXP_47408_1#462" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282526</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#462</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C20, constructed from sample accession ERS13472890 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282763" alias="SC_EXP_47408_1#948" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282763</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#948</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B14, constructed from sample accession ERS13473019 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473019">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282494" alias="SC_EXP_47408_1#430" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282494</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#430</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A12, constructed from sample accession ERS13472780 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472780">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375792</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282468" alias="SC_EXP_47408_1#404" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282468</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#404</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M4, constructed from sample accession ERS13472753 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472753">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472753</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282740" alias="SC_EXP_47408_1#925" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282740</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#925</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L6, constructed from sample accession ERS13473126 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282591" alias="SC_EXP_47408_1#621" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282591</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#621</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H14, constructed from sample accession ERS13473022 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473022">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282677" alias="SC_EXP_47408_1#767" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282677</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#767</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A14, constructed from sample accession ERS13472788 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472788">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282708" alias="SC_EXP_47408_1#798" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282708</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#798</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E22, constructed from sample accession ERS13472897 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472897">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282437" alias="SC_EXP_47408_1#313" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282437</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H20, constructed from sample accession ERS13473043 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282891" alias="SC_EXP_47423_1#150" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282891</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K24, constructed from sample accession ERS13472996 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282547" alias="SC_EXP_47408_1#577" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282547</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#577</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D2, constructed from sample accession ERS13473109 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282696" alias="SC_EXP_47408_1#786" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282696</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#786</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G18, constructed from sample accession ERS13472885 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282355" alias="SC_EXP_47408_1#137" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282355</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M20, constructed from sample accession ERS13472893 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282302" alias="SC_EXP_47408_1#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282302</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O6, constructed from sample accession ERS13472760 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472760">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282317" alias="SC_EXP_47408_1#99" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282317</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M10, constructed from sample accession ERS13472777 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472777">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282979" alias="SC_EXP_47423_1#238" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282979</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J23, constructed from sample accession ERS13472860 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282952" alias="SC_EXP_47423_1#211" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282952</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L15, constructed from sample accession ERS13472833 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472833">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472833</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282629" alias="SC_EXP_47408_1#719" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282629</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#719</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A2, constructed from sample accession ERS13472863 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282379" alias="SC_EXP_47408_1#255" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282379</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D4, constructed from sample accession ERS13473116 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282580" alias="SC_EXP_47408_1#610" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282580</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#610</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N10, constructed from sample accession ERS13473011 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282289" alias="SC_EXP_47408_1#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282289</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E4, constructed from sample accession ERS13472873 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472873">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282859" alias="SC_EXP_47423_1#118" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282859</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A16, constructed from sample accession ERS13472963 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282814" alias="SC_EXP_47423_1#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282814</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G4, constructed from sample accession ERS13472918 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472918">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282645" alias="SC_EXP_47408_1#735" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282645</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#735</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A6, constructed from sample accession ERS13472754 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472754">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282662" alias="SC_EXP_47408_1#752" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282662</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#752</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C10, constructed from sample accession ERS13472775 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472775">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282632" alias="SC_EXP_47408_1#722" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282632</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#722</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G2, constructed from sample accession ERS13472866 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282371" alias="SC_EXP_47408_1#247" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282371</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B2, constructed from sample accession ERS13473112 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282652" alias="SC_EXP_47408_1#742" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282652</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#742</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O6, constructed from sample accession ERS13472760 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472760">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282707" alias="SC_EXP_47408_1#797" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282707</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#797</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C22, constructed from sample accession ERS13472895 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282346" alias="SC_EXP_47408_1#128" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282346</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G18, constructed from sample accession ERS13472885 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472885">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472885</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282447" alias="SC_EXP_47408_1#323" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282447</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D24, constructed from sample accession ERS13473051 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473051">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473051</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282745" alias="SC_EXP_47408_1#930" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282745</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#930</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H8, constructed from sample accession ERS13473131 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282483" alias="SC_EXP_47408_1#419" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282483</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#419</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K8, constructed from sample accession ERS13472768 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472768">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282699" alias="SC_EXP_47408_1#789" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282699</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#789</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M18, constructed from sample accession ERS13472888 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282497" alias="SC_EXP_47408_1#433" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282497</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#433</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G12, constructed from sample accession ERS13472782 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472782">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472782</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282529" alias="SC_EXP_47408_1#465" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282529</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#465</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K20, constructed from sample accession ERS13472894 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472894">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282502" alias="SC_EXP_47408_1#438" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282502</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#438</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A14, constructed from sample accession ERS13472788 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472788">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282678" alias="SC_EXP_47408_1#768" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282678</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#768</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C14, constructed from sample accession ERS13472787 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472787">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282616" alias="SC_EXP_47408_1#646" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282616</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#646</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D22, constructed from sample accession ERS13473047 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282809" alias="SC_EXP_47423_1#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282809</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M2, constructed from sample accession ERS13472914 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282491" alias="SC_EXP_47408_1#427" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282491</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#427</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K10, constructed from sample accession ERS13472776 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472776">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472776</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282445" alias="SC_EXP_47408_1#321" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282445</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L22, constructed from sample accession ERS13473056 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282432" alias="SC_EXP_47408_1#308" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282432</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L18, constructed from sample accession ERS13473038 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473038">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282554" alias="SC_EXP_47408_1#584" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282554</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#584</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D4, constructed from sample accession ERS13473116 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282305" alias="SC_EXP_47408_1#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282305</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E8, constructed from sample accession ERS13472764 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472764">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472764</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282621" alias="SC_EXP_47408_1#651" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282621</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B24, constructed from sample accession ERS13473052 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282873" alias="SC_EXP_47423_1#132" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282873</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A20, constructed from sample accession ERS13472978 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472978">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282384" alias="SC_EXP_47408_1#260" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282384</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N4, constructed from sample accession ERS13473120 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282761" alias="SC_EXP_47408_1#946" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282761</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#946</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L12, constructed from sample accession ERS13473017 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473017">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282948" alias="SC_EXP_47423_1#207" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282948</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D15, constructed from sample accession ERS13472829 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472829">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472829</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282280" alias="SC_EXP_47408_1#62" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282280</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C2, constructed from sample accession ERS13472864 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472864">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282460" alias="SC_EXP_47408_1#396" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282460</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#396</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M2, constructed from sample accession ERS13472872 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472872">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282586" alias="SC_EXP_47408_1#616" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282586</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#616</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L12, constructed from sample accession ERS13473017 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473017">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282615" alias="SC_EXP_47408_1#645" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282615</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#645</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B22, constructed from sample accession ERS13473046 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282655" alias="SC_EXP_47408_1#745" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282655</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#745</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E8, constructed from sample accession ERS13472764 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472764">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472764</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282444" alias="SC_EXP_47408_1#320" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282444</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J22, constructed from sample accession ERS13473050 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473050">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282694" alias="SC_EXP_47408_1#784" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282694</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#784</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C18, constructed from sample accession ERS13472883 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472883">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472883</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282390" alias="SC_EXP_47408_1#266" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282390</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#266</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L6, constructed from sample accession ERS13473126 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282776" alias="SC_EXP_47408_1#961" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282776</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#961</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N16, constructed from sample accession ERS13473031 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473031">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282397" alias="SC_EXP_47408_1#273" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282397</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#273</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L8, constructed from sample accession ERS13473134 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282327" alias="SC_EXP_47408_1#109" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282327</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A14, constructed from sample accession ERS13472788 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472788">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282850" alias="SC_EXP_47423_1#109" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282850</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O12, constructed from sample accession ERS13472955 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472955">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282724" alias="SC_EXP_47408_1#909" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282724</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#909</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H2, constructed from sample accession ERS13473110 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282982" alias="SC_EXP_47423_1#241" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282982</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:P23, constructed from sample accession ERS15395410 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282848" alias="SC_EXP_47423_1#107" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282848</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K12, constructed from sample accession ERS13472953 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282406" alias="SC_EXP_47408_1#282" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282406</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#282</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B12, constructed from sample accession ERS13473012 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473012">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282816" alias="SC_EXP_47423_1#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282816</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K4, constructed from sample accession ERS13472920 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472920">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282606" alias="SC_EXP_47408_1#636" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282606</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#636</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J18, constructed from sample accession ERS13473037 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473037">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282887" alias="SC_EXP_47423_1#146" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282887</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C24, constructed from sample accession ERS13472991 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282749" alias="SC_EXP_47408_1#934" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282749</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#934</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B10, constructed from sample accession ERS13473136 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282314" alias="SC_EXP_47408_1#96" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282314</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G10, constructed from sample accession ERS13472773 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472773">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472773</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282378" alias="SC_EXP_47408_1#254" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282378</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B4, constructed from sample accession ERS13473115 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282405" alias="SC_EXP_47408_1#281" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282405</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#281</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N10, constructed from sample accession ERS13473011 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282705" alias="SC_EXP_47408_1#795" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282705</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#795</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M20, constructed from sample accession ERS13472893 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282892" alias="SC_EXP_47423_1#151" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282892</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M24, constructed from sample accession ERS13472997 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282960" alias="SC_EXP_47423_1#219" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282960</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N17, constructed from sample accession ERS13472840 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472840">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472840</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282736" alias="SC_EXP_47408_1#921" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282736</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#921</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D6, constructed from sample accession ERS13473122 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282385" alias="SC_EXP_47408_1#261" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282385</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B6, constructed from sample accession ERS13473121 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282851" alias="SC_EXP_47423_1#110" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282851</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A14, constructed from sample accession ERS13472959 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472959">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282523" alias="SC_EXP_47408_1#459" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282523</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#459</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K18, constructed from sample accession ERS13472887 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282744" alias="SC_EXP_47408_1#929" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282744</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#929</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F8, constructed from sample accession ERS13473130 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282886" alias="SC_EXP_47423_1#145" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282886</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A24, constructed from sample accession ERS13472992 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472992">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472992</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282734" alias="SC_EXP_47408_1#919" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282734</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#919</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N4, constructed from sample accession ERS13473120 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282780" alias="SC_EXP_47408_1#965" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282780</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#965</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H18, constructed from sample accession ERS13473036 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282812" alias="SC_EXP_47423_1#71" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282812</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#71</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C4, constructed from sample accession ERS13472921 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472921">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472921</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282530" alias="SC_EXP_47408_1#466" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282530</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#466</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M20, constructed from sample accession ERS13472893 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282571" alias="SC_EXP_47408_1#601" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282571</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#601</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J8, constructed from sample accession ERS13473132 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282831" alias="SC_EXP_47423_1#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282831</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I8, constructed from sample accession ERS13472935 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472935">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282946" alias="SC_EXP_47423_1#205" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282946</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#205</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N13, constructed from sample accession ERS13472827 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472827">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472827</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282903" alias="SC_EXP_47423_1#162" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282903</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D3, constructed from sample accession ERS13472739 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472739">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472739</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282426" alias="SC_EXP_47408_1#302" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282426</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N16, constructed from sample accession ERS13473031 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473031">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282667" alias="SC_EXP_47408_1#757" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282667</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#757</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M10, constructed from sample accession ERS13472777 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472777">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282772" alias="SC_EXP_47408_1#957" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282772</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#957</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F16, constructed from sample accession ERS13473032 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282698" alias="SC_EXP_47408_1#788" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282698</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#788</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K18, constructed from sample accession ERS13472887 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282473" alias="SC_EXP_47408_1#409" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282473</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#409</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G6, constructed from sample accession ERS13472758 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472758">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472758</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375769</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282660" alias="SC_EXP_47408_1#750" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282660</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#750</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O8, constructed from sample accession ERS13472770 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472770">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472770</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282440" alias="SC_EXP_47408_1#316" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282440</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B22, constructed from sample accession ERS13473046 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282364" alias="SC_EXP_47408_1#146" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282364</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C24, constructed from sample accession ERS13472901 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472901">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282482" alias="SC_EXP_47408_1#418" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282482</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#418</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I8, constructed from sample accession ERS13472767 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472767">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472767</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282536" alias="SC_EXP_47408_1#472" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282536</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#472</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K22, constructed from sample accession ERS13472902 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282774" alias="SC_EXP_47408_1#959" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282774</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#959</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J16, constructed from sample accession ERS13473029 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282286" alias="SC_EXP_47408_1#68" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282286</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O2, constructed from sample accession ERS13472869 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472869">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282701" alias="SC_EXP_47408_1#791" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282701</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#791</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C20, constructed from sample accession ERS13472890 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282490" alias="SC_EXP_47408_1#426" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282490</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#426</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I10, constructed from sample accession ERS13472774 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472774">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282400" alias="SC_EXP_47408_1#276" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282400</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#276</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D10, constructed from sample accession ERS13473137 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282663" alias="SC_EXP_47408_1#753" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282663</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#753</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E10, constructed from sample accession ERS13472772 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472772">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472772</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282957" alias="SC_EXP_47423_1#216" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282957</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H17, constructed from sample accession ERS13472838 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472838">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282466" alias="SC_EXP_47408_1#402" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282466</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#402</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I4, constructed from sample accession ERS13472875 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472875">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282666" alias="SC_EXP_47408_1#756" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282666</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#756</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K10, constructed from sample accession ERS13472776 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472776">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472776</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282498" alias="SC_EXP_47408_1#434" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282498</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#434</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I12, constructed from sample accession ERS13472783 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472783">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282601" alias="SC_EXP_47408_1#631" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282601</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#631</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N16, constructed from sample accession ERS13473031 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473031">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473031</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282386" alias="SC_EXP_47408_1#262" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282386</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#262</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D6, constructed from sample accession ERS13473122 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473122">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473122</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282500" alias="SC_EXP_47408_1#436" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282500</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#436</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M12, constructed from sample accession ERS13472785 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472785">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472785</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282610" alias="SC_EXP_47408_1#640" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282610</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#640</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D20, constructed from sample accession ERS13473041 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473041">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282519" alias="SC_EXP_47408_1#455" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282519</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#455</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C18, constructed from sample accession ERS13472883 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472883">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472883</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282858" alias="SC_EXP_47423_1#117" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282858</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O14, constructed from sample accession ERS13472962 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282654" alias="SC_EXP_47408_1#744" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282654</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#744</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C8, constructed from sample accession ERS13472763 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472763">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472763</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282959" alias="SC_EXP_47423_1#218" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282959</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L17, constructed from sample accession ERS13472839 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282709" alias="SC_EXP_47408_1#799" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282709</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#799</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G22, constructed from sample accession ERS13472899 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472899">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282313" alias="SC_EXP_47408_1#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282313</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E10, constructed from sample accession ERS13472772 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472772">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472772</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282284" alias="SC_EXP_47408_1#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282284</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K2, constructed from sample accession ERS13472867 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472867">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282429" alias="SC_EXP_47408_1#305" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282429</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F18, constructed from sample accession ERS13473035 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473035">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282637" alias="SC_EXP_47408_1#727" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282637</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#727</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A4, constructed from sample accession ERS13472870 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282683" alias="SC_EXP_47408_1#773" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282683</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#773</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M14, constructed from sample accession ERS13472803 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472803">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472803</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282659" alias="SC_EXP_47408_1#749" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282659</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#749</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M8, constructed from sample accession ERS13472769 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472769">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472769</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282633" alias="SC_EXP_47408_1#723" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282633</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#723</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I2, constructed from sample accession ERS13472868 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472868">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282710" alias="SC_EXP_47408_1#800" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282710</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#800</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I22, constructed from sample accession ERS13472898 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472898">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282348" alias="SC_EXP_47408_1#130" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282348</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K18, constructed from sample accession ERS13472887 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282712" alias="SC_EXP_47408_1#802" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282712</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#802</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M22, constructed from sample accession ERS13472904 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472904">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282376" alias="SC_EXP_47408_1#252" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282376</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L2, constructed from sample accession ERS13473113 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282464" alias="SC_EXP_47408_1#400" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282464</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#400</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E4, constructed from sample accession ERS13472873 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472873">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282801" alias="SC_EXP_47408_1#986" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282801</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#986</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L24, constructed from sample accession ERS13473057 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282727" alias="SC_EXP_47408_1#912" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282727</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#912</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N2, constructed from sample accession ERS13473114 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282587" alias="SC_EXP_47408_1#617" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282587</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#617</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N12, constructed from sample accession ERS13473018 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282978" alias="SC_EXP_47423_1#237" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282978</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H23, constructed from sample accession ERS13472858 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472858">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282578" alias="SC_EXP_47408_1#608" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282578</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#608</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J10, constructed from sample accession ERS13473009 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473009">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282879" alias="SC_EXP_47423_1#138" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282879</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A22, constructed from sample accession ERS13472983 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375995</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282762" alias="SC_EXP_47408_1#947" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282762</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#947</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N12, constructed from sample accession ERS13473018 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282296" alias="SC_EXP_47408_1#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282296</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C6, constructed from sample accession ERS13472756 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472756">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472756</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282872" alias="SC_EXP_47423_1#131" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282872</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K18, constructed from sample accession ERS13472977 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282752" alias="SC_EXP_47408_1#937" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282752</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#937</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H10, constructed from sample accession ERS13473008 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376021</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282945" alias="SC_EXP_47423_1#204" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282945</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L13, constructed from sample accession ERS13472826 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472826">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282923" alias="SC_EXP_47423_1#182" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282923</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L7, constructed from sample accession ERS13472804 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472804">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282756" alias="SC_EXP_47408_1#941" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282756</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#941</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B12, constructed from sample accession ERS13473012 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473012">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282901" alias="SC_EXP_47423_1#160" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282901</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:P1, constructed from sample accession ERS13472737 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472737">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472737</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282682" alias="SC_EXP_47408_1#772" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282682</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#772</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K14, constructed from sample accession ERS13472791 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472791">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472791</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282963" alias="SC_EXP_47423_1#222" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282963</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#222</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F19, constructed from sample accession ERS13472844 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472844">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472844</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282656" alias="SC_EXP_47408_1#746" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282656</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#746</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G8, constructed from sample accession ERS13472765 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472765">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282370" alias="SC_EXP_47408_1#152" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282370</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O24, constructed from sample accession ERS15395411 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282856" alias="SC_EXP_47423_1#115" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282856</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K14, constructed from sample accession ERS13472960 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282511" alias="SC_EXP_47408_1#447" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282511</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#447</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C16, constructed from sample accession ERS13472795 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472795">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472795</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282972" alias="SC_EXP_47423_1#231" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282972</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#231</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J21, constructed from sample accession ERS13472853 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472853">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472853</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282441" alias="SC_EXP_47408_1#317" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282441</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#317</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D22, constructed from sample accession ERS13473047 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282669" alias="SC_EXP_47408_1#759" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282669</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#759</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A12, constructed from sample accession ERS13472780 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472780">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375792</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282674" alias="SC_EXP_47408_1#764" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282674</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#764</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K12, constructed from sample accession ERS13472784 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472784">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282719" alias="SC_EXP_47408_1#809" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282719</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#809</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M24, constructed from sample accession ERS13472908 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282319" alias="SC_EXP_47408_1#101" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282319</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A12, constructed from sample accession ERS13472780 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472780">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375792</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282944" alias="SC_EXP_47423_1#203" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282944</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J13, constructed from sample accession ERS13472824 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472824">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472824</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282517" alias="SC_EXP_47408_1#453" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282517</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#453</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O16, constructed from sample accession ERS13472881 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472881">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472881</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282800" alias="SC_EXP_47408_1#985" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282800</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#985</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J24, constructed from sample accession ERS13473055 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282755" alias="SC_EXP_47408_1#940" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282755</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#940</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N10, constructed from sample accession ERS13473011 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376023</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282301" alias="SC_EXP_47408_1#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282301</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M6, constructed from sample accession ERS13472761 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472761">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472761</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282703" alias="SC_EXP_47408_1#793" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282703</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#793</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I20, constructed from sample accession ERS13472892 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282404" alias="SC_EXP_47408_1#280" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282404</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#280</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L10, constructed from sample accession ERS13473010 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282965" alias="SC_EXP_47423_1#224" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282965</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J19, constructed from sample accession ERS13472846 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472846">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472846</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282315" alias="SC_EXP_47408_1#97" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282315</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I10, constructed from sample accession ERS13472774 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472774">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282351" alias="SC_EXP_47408_1#133" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282351</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C20, constructed from sample accession ERS13472890 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472890">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472890</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282337" alias="SC_EXP_47408_1#119" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282337</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E16, constructed from sample accession ERS13472876 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472876">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282623" alias="SC_EXP_47408_1#653" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282623</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F24, constructed from sample accession ERS13473053 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282807" alias="SC_EXP_47423_1#66" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282807</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#66</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I2, constructed from sample accession ERS13472912 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472912">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282461" alias="SC_EXP_47408_1#397" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282461</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#397</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O2, constructed from sample accession ERS13472869 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472869">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282878" alias="SC_EXP_47423_1#137" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282878</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M20, constructed from sample accession ERS13472985 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282363" alias="SC_EXP_47408_1#145" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282363</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A24, constructed from sample accession ERS13472900 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472900">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282837" alias="SC_EXP_47423_1#96" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282837</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E10, constructed from sample accession ERS13472940 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282636" alias="SC_EXP_47408_1#726" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282636</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#726</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O2, constructed from sample accession ERS13472869 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472869">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282484" alias="SC_EXP_47408_1#420" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282484</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#420</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M8, constructed from sample accession ERS13472769 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472769">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472769</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282791" alias="SC_EXP_47408_1#976" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282791</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#976</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D22, constructed from sample accession ERS13473047 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282971" alias="SC_EXP_47423_1#230" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282971</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H21, constructed from sample accession ERS13472852 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472852">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472852</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282506" alias="SC_EXP_47408_1#442" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282506</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#442</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I14, constructed from sample accession ERS13472790 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472790">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282595" alias="SC_EXP_47408_1#625" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282595</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#625</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B16, constructed from sample accession ERS13473025 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473025">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283412" alias="SC_EXP_47433_1#145" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283412</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#145</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A20, constructed from sample accession ERS13478604 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478604">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478604</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381623</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283191" alias="SC_EXP_47423_1#752" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283191</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#752</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M8, constructed from sample accession ERS13472937 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472937">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283346" alias="SC_EXP_47433_1#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283346</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K2, constructed from sample accession ERS13478538 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478538">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478538</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381559</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283128" alias="SC_EXP_47423_1#538" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283128</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#538</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F15, constructed from sample accession ERS13472830 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472830">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283170" alias="SC_EXP_47423_1#731" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283170</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#731</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C4, constructed from sample accession ERS13472921 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472921">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472921</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283034" alias="SC_EXP_47423_1#444" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283034</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#444</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I14, constructed from sample accession ERS13472961 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283410" alias="SC_EXP_47433_1#143" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283410</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K18, constructed from sample accession ERS13478601 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478601">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478601</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381621</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283186" alias="SC_EXP_47423_1#747" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283186</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#747</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C8, constructed from sample accession ERS13472931 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283280" alias="SC_EXP_47423_1#841" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283280</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#841</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J7, constructed from sample accession ERS13472802 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472802">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283214" alias="SC_EXP_47423_1#775" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283214</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#775</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K14, constructed from sample accession ERS13472960 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283331" alias="SC_EXP_47423_1#893" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283331</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#893</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L21, constructed from sample accession ERS13472854 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283395" alias="SC_EXP_47433_1#128" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283395</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M14, constructed from sample accession ERS13478587 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478587">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478587</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381607</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283432" alias="SC_EXP_47433_1#165" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283432</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#165</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M24, constructed from sample accession ERS13478624 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478624">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478624</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381644</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283120" alias="SC_EXP_47423_1#530" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283120</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#530</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D13, constructed from sample accession ERS13472821 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472821">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472821</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283133" alias="SC_EXP_47423_1#543" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283133</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#543</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B17, constructed from sample accession ERS13472835 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472835">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472835</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283289" alias="SC_EXP_47423_1#850" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283289</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#850</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L9, constructed from sample accession ERS13472812 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472812">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472812</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283181" alias="SC_EXP_47423_1#742" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283181</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#742</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I6, constructed from sample accession ERS13472927 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472927">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472927</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283491" alias="SC_EXP_47433_1#224" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283491</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#224</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H19, constructed from sample accession ERS13473195 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473195">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283511" alias="SC_EXP_47433_1#244" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283511</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#244</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L2, constructed from sample accession ERS13478496 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478496">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478496</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381516</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283296" alias="SC_EXP_47423_1#857" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283296</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#857</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L11, constructed from sample accession ERS13472819 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472819">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283300" alias="SC_EXP_47423_1#861" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283300</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#861</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F13, constructed from sample accession ERS13472822 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472822">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472822</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283097" alias="SC_EXP_47423_1#507" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283097</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#507</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B7, constructed from sample accession ERS13472798 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472798">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283313" alias="SC_EXP_47423_1#874" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283313</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#874</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D17, constructed from sample accession ERS13472836 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472836">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283385" alias="SC_EXP_47433_1#118" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283385</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#118</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I12, constructed from sample accession ERS13478575 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478575">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478575</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283316" alias="SC_EXP_47423_1#877" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283316</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#877</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J17, constructed from sample accession ERS13472842 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283510" alias="SC_EXP_47433_1#243" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283510</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#243</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J2, constructed from sample accession ERS13478495 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478495">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478495</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381515</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283251" alias="SC_EXP_47423_1#812" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283251</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#812</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O24, constructed from sample accession ERS15395412 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283164" alias="SC_EXP_47423_1#725" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283164</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#725</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G2, constructed from sample accession ERS13472910 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472910">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283309" alias="SC_EXP_47423_1#870" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283309</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#870</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J15, constructed from sample accession ERS13472832 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472832">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283521" alias="SC_EXP_47433_1#254" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283521</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#254</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D6, constructed from sample accession ERS13478507 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478507">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478507</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283230" alias="SC_EXP_47423_1#791" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283230</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#791</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K18, constructed from sample accession ERS13472977 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283319" alias="SC_EXP_47423_1#880" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283319</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#880</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B19, constructed from sample accession ERS13472841 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472841">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283019" alias="SC_EXP_47423_1#429" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283019</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#429</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K10, constructed from sample accession ERS13472944 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283499" alias="SC_EXP_47433_1#232" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283499</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B23, constructed from sample accession ERS13473203 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473203">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473203</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283514" alias="SC_EXP_47433_1#247" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283514</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#247</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D4, constructed from sample accession ERS13478504 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478504">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478504</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381524</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283392" alias="SC_EXP_47433_1#125" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283392</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G14, constructed from sample accession ERS13478584 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478584">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478584</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381604</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283436" alias="SC_EXP_47433_1#169" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283436</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F1, constructed from sample accession ERS13473142 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473142">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283029" alias="SC_EXP_47423_1#439" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283029</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#439</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O12, constructed from sample accession ERS13472955 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472955">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283434" alias="SC_EXP_47433_1#167" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283434</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B1, constructed from sample accession ERS13473138 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473138">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283222" alias="SC_EXP_47423_1#783" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283222</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#783</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K16, constructed from sample accession ERS13472968 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283162" alias="SC_EXP_47423_1#723" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283162</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#723</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A2, constructed from sample accession ERS13472909 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472909">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472909</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283407" alias="SC_EXP_47433_1#140" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283407</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E18, constructed from sample accession ERS13478596 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478596">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478596</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381616</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283001" alias="SC_EXP_47423_1#411" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283001</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#411</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G6, constructed from sample accession ERS13472938 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283490" alias="SC_EXP_47433_1#223" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283490</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F19, constructed from sample accession ERS13473194 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473194">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473194</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376207</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283342" alias="SC_EXP_47433_1#75" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283342</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C2, constructed from sample accession ERS13478534 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478534">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478534</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381554</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283258" alias="SC_EXP_47423_1#819" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283258</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#819</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N1, constructed from sample accession ERS13472736 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472736">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472736</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283476" alias="SC_EXP_47433_1#209" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283476</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B15, constructed from sample accession ERS13473180 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473180">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473180</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283503" alias="SC_EXP_47433_1#236" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283503</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#236</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J23, constructed from sample accession ERS13473206 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473206">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473206</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283451" alias="SC_EXP_47433_1#184" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283451</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#184</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L5, constructed from sample accession ERS13473155 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473155">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283179" alias="SC_EXP_47423_1#740" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283179</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#740</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E6, constructed from sample accession ERS13472924 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472924">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472924</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283163" alias="SC_EXP_47423_1#724" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283163</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#724</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C2, constructed from sample accession ERS13472911 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283270" alias="SC_EXP_47423_1#831" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283270</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#831</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F5, constructed from sample accession ERS13472749 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472749">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472749</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283286" alias="SC_EXP_47423_1#847" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283286</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#847</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F9, constructed from sample accession ERS13472809 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472809">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472809</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283285" alias="SC_EXP_47423_1#846" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283285</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#846</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D9, constructed from sample accession ERS13472808 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472808">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283221" alias="SC_EXP_47423_1#782" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283221</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#782</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I16, constructed from sample accession ERS13472967 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283048" alias="SC_EXP_47423_1#458" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283048</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#458</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E18, constructed from sample accession ERS13472974 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283176" alias="SC_EXP_47423_1#737" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283176</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#737</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O4, constructed from sample accession ERS13472933 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472933">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283423" alias="SC_EXP_47433_1#156" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283423</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I22, constructed from sample accession ERS13478615 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478615">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478615</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381635</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283475" alias="SC_EXP_47433_1#208" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283475</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L13, constructed from sample accession ERS13473179 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473179">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282998" alias="SC_EXP_47423_1#408" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282998</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#408</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A6, constructed from sample accession ERS13472922 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472922">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283367" alias="SC_EXP_47433_1#100" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283367</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E8, constructed from sample accession ERS13478559 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478559">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478559</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381579</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283235" alias="SC_EXP_47423_1#796" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283235</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#796</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K20, constructed from sample accession ERS13472982 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472982">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375994</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283011" alias="SC_EXP_47423_1#421" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283011</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#421</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K8, constructed from sample accession ERS13472936 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472936">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472936</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283238" alias="SC_EXP_47423_1#799" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283238</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#799</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C22, constructed from sample accession ERS13472987 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283148" alias="SC_EXP_47423_1#558" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283148</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#558</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D21, constructed from sample accession ERS13472850 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472850">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472850</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283519" alias="SC_EXP_47433_1#252" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283519</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#252</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:N4, constructed from sample accession ERS13478505 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478505">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478505</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283445" alias="SC_EXP_47433_1#178" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283445</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#178</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L3, constructed from sample accession ERS13473149 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473149">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283084" alias="SC_EXP_47423_1#494" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283084</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#494</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H3, constructed from sample accession ERS13472741 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472741">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472741</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283478" alias="SC_EXP_47433_1#211" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283478</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#211</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F15, constructed from sample accession ERS13473182 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473182">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473182</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376194</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283178" alias="SC_EXP_47423_1#739" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283178</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#739</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C6, constructed from sample accession ERS13472925 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283322" alias="SC_EXP_47423_1#883" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283322</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#883</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H19, constructed from sample accession ERS13472845 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283205" alias="SC_EXP_47423_1#766" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283205</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#766</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I12, constructed from sample accession ERS13472952 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283336" alias="SC_EXP_47423_1#898" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283336</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#898</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H23, constructed from sample accession ERS13472858 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472858">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283248" alias="SC_EXP_47423_1#809" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283248</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#809</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I24, constructed from sample accession ERS13472995 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283111" alias="SC_EXP_47423_1#521" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283111</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#521</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N9, constructed from sample accession ERS13472813 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472813">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472813</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283125" alias="SC_EXP_47423_1#535" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283125</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#535</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N13, constructed from sample accession ERS13472827 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472827">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472827</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283085" alias="SC_EXP_47423_1#495" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283085</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#495</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J3, constructed from sample accession ERS13472742 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472742">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472742</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283266" alias="SC_EXP_47423_1#827" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283266</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#827</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N3, constructed from sample accession ERS13472743 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472743">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472743</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283284" alias="SC_EXP_47423_1#845" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283284</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#845</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B9, constructed from sample accession ERS13472807 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472807">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472807</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283389" alias="SC_EXP_47433_1#122" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283389</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#122</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A14, constructed from sample accession ERS13478581 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478581">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478581</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283249" alias="SC_EXP_47423_1#810" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283249</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#810</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K24, constructed from sample accession ERS13472996 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282999" alias="SC_EXP_47423_1#409" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282999</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#409</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C6, constructed from sample accession ERS13472925 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283095" alias="SC_EXP_47423_1#505" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283095</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#505</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N5, constructed from sample accession ERS13472796 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472796">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283060" alias="SC_EXP_47423_1#470" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283060</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#470</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E22, constructed from sample accession ERS13472984 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283350" alias="SC_EXP_47433_1#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283350</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C4, constructed from sample accession ERS13478542 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478542">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478542</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381562</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283105" alias="SC_EXP_47423_1#515" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283105</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#515</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B9, constructed from sample accession ERS13472807 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472807">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472807</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283026" alias="SC_EXP_47423_1#436" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283026</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#436</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I12, constructed from sample accession ERS13472952 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283053" alias="SC_EXP_47423_1#463" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283053</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#463</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E20, constructed from sample accession ERS13472979 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472979">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283333" alias="SC_EXP_47423_1#895" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283333</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#895</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B23, constructed from sample accession ERS13472856 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472856">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472856</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282990" alias="SC_EXP_47423_1#400" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282990</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#400</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A4, constructed from sample accession ERS13472916 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472916">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283185" alias="SC_EXP_47423_1#746" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283185</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#746</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A8, constructed from sample accession ERS13472929 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472929">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283044" alias="SC_EXP_47423_1#454" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283044</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#454</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M16, constructed from sample accession ERS13472970 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283069" alias="SC_EXP_47423_1#479" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283069</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#479</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I24, constructed from sample accession ERS13472995 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283425" alias="SC_EXP_47433_1#158" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283425</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M22, constructed from sample accession ERS13478617 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478617">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478617</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381637</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283427" alias="SC_EXP_47433_1#160" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283427</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#160</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C24, constructed from sample accession ERS13478619 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478619">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478619</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381639</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283447" alias="SC_EXP_47433_1#180" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283447</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D5, constructed from sample accession ERS13473151 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473151">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283494" alias="SC_EXP_47433_1#227" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283494</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B21, constructed from sample accession ERS13473198 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473198">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473198</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283056" alias="SC_EXP_47423_1#466" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283056</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#466</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K20, constructed from sample accession ERS13472982 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472982">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375994</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283381" alias="SC_EXP_47433_1#114" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283381</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A12, constructed from sample accession ERS13478574 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478574">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478574</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283240" alias="SC_EXP_47423_1#801" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283240</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#801</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G22, constructed from sample accession ERS13472986 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283104" alias="SC_EXP_47423_1#514" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283104</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#514</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:P7, constructed from sample accession ERS13472805 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472805">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:P7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283247" alias="SC_EXP_47423_1#808" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283247</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#808</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G24, constructed from sample accession ERS13472994 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283379" alias="SC_EXP_47433_1#112" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283379</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M10, constructed from sample accession ERS13478571 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478571">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478571</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381591</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283035" alias="SC_EXP_47423_1#445" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283035</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#445</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K14, constructed from sample accession ERS13472960 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283442" alias="SC_EXP_47433_1#175" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283442</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F3, constructed from sample accession ERS13473146 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473146">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283223" alias="SC_EXP_47423_1#784" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283223</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#784</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M16, constructed from sample accession ERS13472970 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283353" alias="SC_EXP_47433_1#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283353</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I4, constructed from sample accession ERS13478545 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478545">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478545</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381565</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283485" alias="SC_EXP_47433_1#218" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283485</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#218</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H17, constructed from sample accession ERS13473189 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473189">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473189</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283072" alias="SC_EXP_47423_1#482" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283072</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#482</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O24, constructed from sample accession ERS15395412 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283115" alias="SC_EXP_47423_1#525" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283115</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#525</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H11, constructed from sample accession ERS13472817 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472817">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283153" alias="SC_EXP_47423_1#563" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283153</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#563</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N21, constructed from sample accession ERS13472855 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472855">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472855</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283217" alias="SC_EXP_47423_1#778" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283217</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#778</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A16, constructed from sample accession ERS13472963 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283143" alias="SC_EXP_47423_1#553" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283143</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#553</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H19, constructed from sample accession ERS13472845 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283047" alias="SC_EXP_47423_1#457" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283047</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#457</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C18, constructed from sample accession ERS13472973 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472973">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283361" alias="SC_EXP_47433_1#94" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283361</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I6, constructed from sample accession ERS13478553 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478553">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478553</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381573</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283140" alias="SC_EXP_47423_1#550" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283140</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#550</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B19, constructed from sample accession ERS13472841 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472841">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283430" alias="SC_EXP_47433_1#163" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283430</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#163</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I24, constructed from sample accession ERS13478622 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478622">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478622</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381642</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283187" alias="SC_EXP_47423_1#748" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283187</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#748</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E8, constructed from sample accession ERS13472934 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283277" alias="SC_EXP_47423_1#838" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283277</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#838</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D7, constructed from sample accession ERS13472799 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472799">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283241" alias="SC_EXP_47423_1#802" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283241</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#802</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I22, constructed from sample accession ERS13472989 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283030" alias="SC_EXP_47423_1#440" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283030</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#440</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A14, constructed from sample accession ERS13472959 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472959">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283292" alias="SC_EXP_47423_1#853" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283292</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#853</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D11, constructed from sample accession ERS13472815 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472815">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472815</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283465" alias="SC_EXP_47433_1#198" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283465</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#198</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D11, constructed from sample accession ERS13473168 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473168">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283253" alias="SC_EXP_47423_1#814" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283253</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#814</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D1, constructed from sample accession ERS13472733 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472733">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472733</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283452" alias="SC_EXP_47433_1#185" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283452</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B7, constructed from sample accession ERS13473156 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473156">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283126" alias="SC_EXP_47423_1#536" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283126</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#536</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B15, constructed from sample accession ERS13472828 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283155" alias="SC_EXP_47423_1#565" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283155</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#565</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D23, constructed from sample accession ERS13472861 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472861">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283393" alias="SC_EXP_47433_1#126" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283393</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I14, constructed from sample accession ERS13478585 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478585">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478585</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283180" alias="SC_EXP_47423_1#741" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283180</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#741</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G6, constructed from sample accession ERS13472938 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283450" alias="SC_EXP_47433_1#183" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283450</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#183</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J5, constructed from sample accession ERS13473154 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473154">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283166" alias="SC_EXP_47423_1#727" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283166</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#727</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K2, constructed from sample accession ERS13472913 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472913">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283093" alias="SC_EXP_47423_1#503" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283093</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#503</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J5, constructed from sample accession ERS13472748 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472748">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283411" alias="SC_EXP_47433_1#144" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283411</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M18, constructed from sample accession ERS13478602 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478602">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478602</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381622</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283404" alias="SC_EXP_47433_1#137" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283404</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#137</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O16, constructed from sample accession ERS13478599 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478599">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478599</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381619</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283504" alias="SC_EXP_47433_1#237" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283504</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#237</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:N23, constructed from sample accession ERS15395417 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400270</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283036" alias="SC_EXP_47423_1#446" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283036</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#446</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M14, constructed from sample accession ERS13472964 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283274" alias="SC_EXP_47423_1#835" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283274</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#835</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N5, constructed from sample accession ERS13472796 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472796">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283397" alias="SC_EXP_47433_1#130" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283397</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A16, constructed from sample accession ERS13478589 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478589">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478589</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381610</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283272" alias="SC_EXP_47423_1#833" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283272</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#833</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J5, constructed from sample accession ERS13472748 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472748">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282983" alias="SC_EXP_47423_1#393" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282983</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#393</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A2, constructed from sample accession ERS13472909 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472909">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472909</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283409" alias="SC_EXP_47433_1#142" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283409</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I18, constructed from sample accession ERS13478603 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478603">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478603</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381624</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283107" alias="SC_EXP_47423_1#517" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283107</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#517</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F9, constructed from sample accession ERS13472809 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472809">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472809</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283455" alias="SC_EXP_47433_1#188" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283455</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#188</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H7, constructed from sample accession ERS13473159 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473159">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283252" alias="SC_EXP_47423_1#813" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283252</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#813</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B1, constructed from sample accession ERS13472730 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472730">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472730</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283023" alias="SC_EXP_47423_1#433" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283023</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#433</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C12, constructed from sample accession ERS13472949 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283275" alias="SC_EXP_47423_1#836" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283275</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#836</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:P5, constructed from sample accession ERS13472797 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472797">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:P5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283189" alias="SC_EXP_47423_1#750" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283189</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#750</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I8, constructed from sample accession ERS13472935 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472935">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283211" alias="SC_EXP_47423_1#772" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283211</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#772</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E14, constructed from sample accession ERS13472957 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472957">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283049" alias="SC_EXP_47423_1#459" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283049</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#459</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G18, constructed from sample accession ERS13472975 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283311" alias="SC_EXP_47423_1#872" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283311</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#872</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N15, constructed from sample accession ERS13472834 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472834">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283057" alias="SC_EXP_47423_1#467" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283057</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#467</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M20, constructed from sample accession ERS13472985 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283517" alias="SC_EXP_47433_1#250" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283517</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#250</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J4, constructed from sample accession ERS13478502 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478502">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478502</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381523</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282991" alias="SC_EXP_47423_1#401" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282991</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#401</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C4, constructed from sample accession ERS13472921 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472921">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472921</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283345" alias="SC_EXP_47433_1#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283345</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I2, constructed from sample accession ERS13478537 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478537">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478537</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381557</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283184" alias="SC_EXP_47423_1#745" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283184</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#745</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O6, constructed from sample accession ERS13472928 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283122" alias="SC_EXP_47423_1#532" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283122</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#532</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H13, constructed from sample accession ERS13472823 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472823">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472823</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283339" alias="SC_EXP_47423_1#901" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283339</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#901</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N23, constructed from sample accession ERS13472862 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472862">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283526" alias="SC_EXP_47433_1#259" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283526</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#259</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:N6, constructed from sample accession ERS13478512 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283496" alias="SC_EXP_47433_1#229" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283496</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#229</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F21, constructed from sample accession ERS13473200 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473200">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473200</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376212</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283518" alias="SC_EXP_47433_1#251" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283518</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#251</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L4, constructed from sample accession ERS13478503 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478503">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478503</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381522</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283390" alias="SC_EXP_47433_1#123" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283390</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C14, constructed from sample accession ERS13478582 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478582">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478582</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283505" alias="SC_EXP_47433_1#238" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283505</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#238</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:P23, constructed from sample accession ERS15395418 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283356" alias="SC_EXP_47433_1#89" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283356</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O4, constructed from sample accession ERS13478548 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478548">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478548</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283101" alias="SC_EXP_47423_1#511" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283101</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#511</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J7, constructed from sample accession ERS13472802 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472802">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283108" alias="SC_EXP_47423_1#518" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283108</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#518</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H9, constructed from sample accession ERS13472810 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472810">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472810</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283291" alias="SC_EXP_47423_1#852" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283291</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#852</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B11, constructed from sample accession ERS13472814 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283083" alias="SC_EXP_47423_1#493" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283083</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#493</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F3, constructed from sample accession ERS13472740 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472740">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472740</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283231" alias="SC_EXP_47423_1#792" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283231</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#792</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A20, constructed from sample accession ERS13472978 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472978">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283144" alias="SC_EXP_47423_1#554" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283144</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#554</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J19, constructed from sample accession ERS13472846 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472846">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472846</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283228" alias="SC_EXP_47423_1#789" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283228</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#789</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G18, constructed from sample accession ERS13472975 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472975">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472975</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283360" alias="SC_EXP_47433_1#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283360</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G6, constructed from sample accession ERS13478551 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478551">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478551</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283200" alias="SC_EXP_47423_1#761" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283200</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#761</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O10, constructed from sample accession ERS13472947 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283325" alias="SC_EXP_47423_1#886" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283325</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#886</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N19, constructed from sample accession ERS13472848 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283050" alias="SC_EXP_47423_1#460" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283050</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#460</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I18, constructed from sample accession ERS13472976 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472976">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283086" alias="SC_EXP_47423_1#496" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283086</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#496</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L3, constructed from sample accession ERS13472745 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472745">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283175" alias="SC_EXP_47423_1#736" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283175</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#736</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M4, constructed from sample accession ERS13472923 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472923">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472923</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283197" alias="SC_EXP_47423_1#758" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283197</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#758</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I10, constructed from sample accession ERS13472943 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283299" alias="SC_EXP_47423_1#860" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283299</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#860</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D13, constructed from sample accession ERS13472821 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472821">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472821</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283348" alias="SC_EXP_47433_1#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283348</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O2, constructed from sample accession ERS13478540 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478540">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478540</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381560</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283068" alias="SC_EXP_47423_1#478" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283068</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#478</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G24, constructed from sample accession ERS13472994 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283150" alias="SC_EXP_47423_1#560" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283150</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#560</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H21, constructed from sample accession ERS13472852 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472852">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472852</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283413" alias="SC_EXP_47433_1#146" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283413</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#146</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C20, constructed from sample accession ERS13478605 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478605">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478605</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381625</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282988" alias="SC_EXP_47423_1#398" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282988</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#398</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M2, constructed from sample accession ERS13472914 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283282" alias="SC_EXP_47423_1#843" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283282</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#843</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N7, constructed from sample accession ERS13472806 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472806">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472806</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283124" alias="SC_EXP_47423_1#534" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283124</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#534</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L13, constructed from sample accession ERS13472826 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472826">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283226" alias="SC_EXP_47423_1#787" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283226</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#787</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C18, constructed from sample accession ERS13472973 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472973">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472973</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283279" alias="SC_EXP_47423_1#840" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283279</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#840</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H7, constructed from sample accession ERS13472801 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472801">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283210" alias="SC_EXP_47423_1#771" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283210</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#771</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C14, constructed from sample accession ERS13472956 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283135" alias="SC_EXP_47423_1#545" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283135</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#545</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F17, constructed from sample accession ERS13472837 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472837">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472837</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283168" alias="SC_EXP_47423_1#729" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283168</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#729</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O2, constructed from sample accession ERS13472915 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472915">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283129" alias="SC_EXP_47423_1#539" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283129</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#539</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H15, constructed from sample accession ERS13472831 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283264" alias="SC_EXP_47423_1#825" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283264</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#825</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J3, constructed from sample accession ERS13472742 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472742">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472742</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283332" alias="SC_EXP_47423_1#894" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283332</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#894</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N21, constructed from sample accession ERS13472855 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472855">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472855</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283110" alias="SC_EXP_47423_1#520" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283110</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#520</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L9, constructed from sample accession ERS13472812 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472812">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472812</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283259" alias="SC_EXP_47423_1#820" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283259</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#820</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:P1, constructed from sample accession ERS13472737 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472737">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472737</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283032" alias="SC_EXP_47423_1#442" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283032</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#442</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E14, constructed from sample accession ERS13472957 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472957">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283315" alias="SC_EXP_47423_1#876" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283315</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#876</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H17, constructed from sample accession ERS13472838 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472838">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283295" alias="SC_EXP_47423_1#856" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283295</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#856</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J11, constructed from sample accession ERS13472818 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472818">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472818</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283383" alias="SC_EXP_47433_1#116" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283383</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E12, constructed from sample accession ERS13478576 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478576">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478576</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283364" alias="SC_EXP_47433_1#97" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283364</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#97</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O6, constructed from sample accession ERS13478556 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478556">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478556</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381576</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283527" alias="SC_EXP_47433_1#260" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283527</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#260</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B8, constructed from sample accession ERS13478513 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478513">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283308" alias="SC_EXP_47423_1#869" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283308</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#869</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H15, constructed from sample accession ERS13472831 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283358" alias="SC_EXP_47433_1#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283358</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C6, constructed from sample accession ERS13478550 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478550">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478550</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381570</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283343" alias="SC_EXP_47433_1#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283343</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E2, constructed from sample accession ERS13478535 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478535">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478535</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381555</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283456" alias="SC_EXP_47433_1#189" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283456</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J7, constructed from sample accession ERS13473160 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473160">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473160</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283446" alias="SC_EXP_47433_1#179" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283446</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#179</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B5, constructed from sample accession ERS13473150 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283377" alias="SC_EXP_47433_1#110" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283377</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I10, constructed from sample accession ERS13478568 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478568">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478568</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381588</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283468" alias="SC_EXP_47433_1#201" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283468</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#201</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J11, constructed from sample accession ERS13473173 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473173">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283373" alias="SC_EXP_47433_1#106" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283373</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A10, constructed from sample accession ERS13478565 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478565">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478565</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381584</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283114" alias="SC_EXP_47423_1#524" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283114</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#524</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F11, constructed from sample accession ERS13472816 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472816">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283149" alias="SC_EXP_47423_1#559" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283149</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#559</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F21, constructed from sample accession ERS13472851 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283012" alias="SC_EXP_47423_1#422" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283012</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#422</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M8, constructed from sample accession ERS13472937 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472937">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283387" alias="SC_EXP_47433_1#120" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283387</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M12, constructed from sample accession ERS13478578 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478578">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478578</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283192" alias="SC_EXP_47423_1#753" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283192</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#753</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O8, constructed from sample accession ERS13472946 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283042" alias="SC_EXP_47423_1#452" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283042</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#452</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I16, constructed from sample accession ERS13472967 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283320" alias="SC_EXP_47423_1#881" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283320</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#881</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D19, constructed from sample accession ERS13472843 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472843">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283219" alias="SC_EXP_47423_1#780" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283219</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#780</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E16, constructed from sample accession ERS13472969 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283202" alias="SC_EXP_47423_1#763" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283202</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#763</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C12, constructed from sample accession ERS13472949 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283139" alias="SC_EXP_47423_1#549" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283139</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#549</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N17, constructed from sample accession ERS13472840 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472840">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472840</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283043" alias="SC_EXP_47423_1#453" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283043</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#453</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K16, constructed from sample accession ERS13472968 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283225" alias="SC_EXP_47423_1#786" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283225</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#786</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A18, constructed from sample accession ERS13472972 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472972">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283004" alias="SC_EXP_47423_1#414" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283004</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#414</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M6, constructed from sample accession ERS13472930 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472930">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472930</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283236" alias="SC_EXP_47423_1#797" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283236</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#797</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M20, constructed from sample accession ERS13472985 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283441" alias="SC_EXP_47433_1#174" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283441</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D3, constructed from sample accession ERS13473143 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473143">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283265" alias="SC_EXP_47423_1#826" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283265</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#826</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L3, constructed from sample accession ERS13472745 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472745">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283457" alias="SC_EXP_47433_1#190" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283457</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#190</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L7, constructed from sample accession ERS13473161 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473161">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283080" alias="SC_EXP_47423_1#490" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283080</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#490</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:P1, constructed from sample accession ERS13472737 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472737">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472737</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:P1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283007" alias="SC_EXP_47423_1#417" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283007</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#417</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C8, constructed from sample accession ERS13472931 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283477" alias="SC_EXP_47433_1#210" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283477</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D15, constructed from sample accession ERS13473181 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473181">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473181</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376193</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283256" alias="SC_EXP_47423_1#817" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283256</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#817</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J1, constructed from sample accession ERS13472734 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472734">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472734</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283431" alias="SC_EXP_47433_1#164" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283431</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K24, constructed from sample accession ERS13478623 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478623">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478623</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381643</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283302" alias="SC_EXP_47423_1#863" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283302</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#863</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J13, constructed from sample accession ERS13472824 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472824">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472824</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283151" alias="SC_EXP_47423_1#561" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283151</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#561</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J21, constructed from sample accession ERS13472853 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472853">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472853</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283005" alias="SC_EXP_47423_1#415" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283005</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#415</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O6, constructed from sample accession ERS13472928 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283198" alias="SC_EXP_47423_1#759" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283198</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#759</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K10, constructed from sample accession ERS13472944 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283365" alias="SC_EXP_47433_1#98" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283365</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A8, constructed from sample accession ERS13478557 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478557">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478557</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381577</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283481" alias="SC_EXP_47433_1#214" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283481</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L15, constructed from sample accession ERS13473186 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473186">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283327" alias="SC_EXP_47423_1#889" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283327</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#889</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D21, constructed from sample accession ERS13472850 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472850">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472850</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283209" alias="SC_EXP_47423_1#770" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283209</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#770</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A14, constructed from sample accession ERS13472959 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472959">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472959</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283399" alias="SC_EXP_47433_1#132" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283399</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E16, constructed from sample accession ERS13478592 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478592">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478592</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381612</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283062" alias="SC_EXP_47423_1#472" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283062</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#472</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I22, constructed from sample accession ERS13472989 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283229" alias="SC_EXP_47423_1#790" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283229</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#790</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I18, constructed from sample accession ERS13472976 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472976">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283492" alias="SC_EXP_47433_1#225" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283492</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J19, constructed from sample accession ERS13473196 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473196">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473196</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376208</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283416" alias="SC_EXP_47433_1#149" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283416</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I20, constructed from sample accession ERS13478608 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478608">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478608</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381628</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283470" alias="SC_EXP_47433_1#203" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283470</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#203</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B13, constructed from sample accession ERS13473174 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473174">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283338" alias="SC_EXP_47423_1#900" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283338</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#900</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L23, constructed from sample accession ERS13472859 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472859">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283374" alias="SC_EXP_47433_1#107" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283374</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C10, constructed from sample accession ERS13478569 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478569">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478569</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381589</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283428" alias="SC_EXP_47433_1#161" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283428</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#161</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E24, constructed from sample accession ERS13478620 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478620">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478620</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381640</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283341" alias="SC_EXP_47433_1#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283341</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A2, constructed from sample accession ERS13478533 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478533">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478533</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381553</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283014" alias="SC_EXP_47423_1#424" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283014</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#424</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A10, constructed from sample accession ERS13472941 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283177" alias="SC_EXP_47423_1#738" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283177</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#738</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A6, constructed from sample accession ERS13472922 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472922">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283528" alias="SC_EXP_47433_1#261" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283528</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#261</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D8, constructed from sample accession ERS13478514 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478514">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478514</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283269" alias="SC_EXP_47423_1#830" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283269</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#830</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D5, constructed from sample accession ERS13472755 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472755">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472755</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375768</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283417" alias="SC_EXP_47433_1#150" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283417</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K20, constructed from sample accession ERS13478609 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478609">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478609</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381629</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283203" alias="SC_EXP_47423_1#764" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283203</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#764</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E12, constructed from sample accession ERS13472950 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283453" alias="SC_EXP_47433_1#186" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283453</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D7, constructed from sample accession ERS13473157 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473157">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283075" alias="SC_EXP_47423_1#485" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283075</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#485</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F1, constructed from sample accession ERS13472731 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472731">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283169" alias="SC_EXP_47423_1#730" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283169</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#730</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A4, constructed from sample accession ERS13472916 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472916">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283220" alias="SC_EXP_47423_1#781" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283220</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#781</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G16, constructed from sample accession ERS13472966 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283117" alias="SC_EXP_47423_1#527" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283117</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#527</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L11, constructed from sample accession ERS13472819 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472819">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283165" alias="SC_EXP_47423_1#726" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283165</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#726</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I2, constructed from sample accession ERS13472912 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472912">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283480" alias="SC_EXP_47433_1#213" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283480</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#213</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J15, constructed from sample accession ERS13473184 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473184">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376196</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283250" alias="SC_EXP_47423_1#811" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283250</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#811</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M24, constructed from sample accession ERS13472997 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282997" alias="SC_EXP_47423_1#407" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282997</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#407</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O4, constructed from sample accession ERS13472933 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472933">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472933</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283334" alias="SC_EXP_47423_1#896" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283334</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#896</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D23, constructed from sample accession ERS13472861 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472861">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283182" alias="SC_EXP_47423_1#743" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283182</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#743</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K6, constructed from sample accession ERS13472926 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472926">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472926</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283008" alias="SC_EXP_47423_1#418" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283008</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#418</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E8, constructed from sample accession ERS13472934 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283307" alias="SC_EXP_47423_1#868" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283307</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#868</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F15, constructed from sample accession ERS13472830 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472830">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283520" alias="SC_EXP_47433_1#253" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283520</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#253</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B6, constructed from sample accession ERS13478506 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478506">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478506</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283071" alias="SC_EXP_47423_1#481" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283071</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#481</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M24, constructed from sample accession ERS13472997 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283437" alias="SC_EXP_47433_1#170" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283437</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#170</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H1, constructed from sample accession ERS13473140 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473140">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283158" alias="SC_EXP_47423_1#568" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283158</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#568</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J23, constructed from sample accession ERS13472860 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283354" alias="SC_EXP_47433_1#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283354</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K4, constructed from sample accession ERS13478546 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478546">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478546</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381566</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283328" alias="SC_EXP_47423_1#890" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283328</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#890</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F21, constructed from sample accession ERS13472851 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283359" alias="SC_EXP_47433_1#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283359</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E6, constructed from sample accession ERS13478552 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478552">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478552</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381572</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283438" alias="SC_EXP_47433_1#171" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283438</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#171</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J1, constructed from sample accession ERS13473141 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473141">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283094" alias="SC_EXP_47423_1#504" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283094</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#504</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L5, constructed from sample accession ERS13472750 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472750">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472750</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283290" alias="SC_EXP_47423_1#851" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283290</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#851</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N9, constructed from sample accession ERS13472813 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472813">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472813</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283059" alias="SC_EXP_47423_1#469" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283059</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#469</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C22, constructed from sample accession ERS13472987 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283298" alias="SC_EXP_47423_1#859" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283298</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#859</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B13, constructed from sample accession ERS13472825 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472825">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283031" alias="SC_EXP_47423_1#441" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283031</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#441</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C14, constructed from sample accession ERS13472956 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283112" alias="SC_EXP_47423_1#522" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283112</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#522</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B11, constructed from sample accession ERS13472814 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283375" alias="SC_EXP_47433_1#108" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283375</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E10, constructed from sample accession ERS13478566 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478566">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478566</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381586</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283326" alias="SC_EXP_47423_1#887" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283326</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#887</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B21, constructed from sample accession ERS13472849 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472849">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472849</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283079" alias="SC_EXP_47423_1#489" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283079</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#489</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N1, constructed from sample accession ERS13472736 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472736">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472736</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283516" alias="SC_EXP_47433_1#249" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283516</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H4, constructed from sample accession ERS13478501 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478501">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478501</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381521</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283317" alias="SC_EXP_47423_1#878" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283317</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#878</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L17, constructed from sample accession ERS13472839 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283351" alias="SC_EXP_47433_1#84" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283351</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#84</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E4, constructed from sample accession ERS13478543 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478543">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478543</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381563</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283087" alias="SC_EXP_47423_1#497" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283087</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#497</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N3, constructed from sample accession ERS13472743 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472743">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472743</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283429" alias="SC_EXP_47433_1#162" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283429</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#162</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G24, constructed from sample accession ERS13478621 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478621">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478621</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381641</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283261" alias="SC_EXP_47423_1#822" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283261</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#822</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D3, constructed from sample accession ERS13472739 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472739">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472739</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283509" alias="SC_EXP_47433_1#242" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283509</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#242</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H2, constructed from sample accession ERS13478494 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478494">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478494</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381514</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283058" alias="SC_EXP_47423_1#468" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283058</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#468</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A22, constructed from sample accession ERS13472983 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375995</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283474" alias="SC_EXP_47433_1#207" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283474</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#207</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J13, constructed from sample accession ERS13473178 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473178">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283208" alias="SC_EXP_47423_1#769" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283208</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#769</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O12, constructed from sample accession ERS13472955 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472955">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472955</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283232" alias="SC_EXP_47423_1#793" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283232</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#793</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E20, constructed from sample accession ERS13472979 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472979">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472979</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283141" alias="SC_EXP_47423_1#551" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283141</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#551</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D19, constructed from sample accession ERS13472843 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472843">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283271" alias="SC_EXP_47423_1#832" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283271</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#832</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H5, constructed from sample accession ERS13472747 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472747">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472747</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283207" alias="SC_EXP_47423_1#768" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283207</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#768</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M12, constructed from sample accession ERS13472954 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283362" alias="SC_EXP_47433_1#95" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283362</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#95</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K6, constructed from sample accession ERS13478554 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478554">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478554</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381574</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282989" alias="SC_EXP_47423_1#399" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282989</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#399</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O2, constructed from sample accession ERS13472915 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472915">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283421" alias="SC_EXP_47433_1#154" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283421</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E22, constructed from sample accession ERS13478613 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478613">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478613</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381633</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283077" alias="SC_EXP_47423_1#487" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283077</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#487</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J1, constructed from sample accession ERS13472734 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472734">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472734</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283127" alias="SC_EXP_47423_1#537" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283127</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#537</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D15, constructed from sample accession ERS13472829 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472829">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472829</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283363" alias="SC_EXP_47433_1#96" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283363</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#96</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M6, constructed from sample accession ERS13478555 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478555">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478555</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381575</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283174" alias="SC_EXP_47423_1#735" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283174</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#735</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K4, constructed from sample accession ERS13472920 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472920">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283493" alias="SC_EXP_47433_1#226" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283493</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#226</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L19, constructed from sample accession ERS13473197 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473197">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473197</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376209</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282995" alias="SC_EXP_47423_1#405" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282995</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#405</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K4, constructed from sample accession ERS13472920 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472920">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282992" alias="SC_EXP_47423_1#402" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282992</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#402</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E4, constructed from sample accession ERS13472917 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283138" alias="SC_EXP_47423_1#548" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283138</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#548</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L17, constructed from sample accession ERS13472839 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283142" alias="SC_EXP_47423_1#552" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283142</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#552</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F19, constructed from sample accession ERS13472844 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472844">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472844</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283020" alias="SC_EXP_47423_1#430" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283020</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#430</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M10, constructed from sample accession ERS13472945 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283242" alias="SC_EXP_47423_1#803" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283242</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#803</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K22, constructed from sample accession ERS13472988 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283398" alias="SC_EXP_47433_1#131" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283398</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C16, constructed from sample accession ERS13478590 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478590">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478590</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381609</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283418" alias="SC_EXP_47433_1#151" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283418</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M20, constructed from sample accession ERS13478610 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478610">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478610</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381627</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283524" alias="SC_EXP_47433_1#257" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283524</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J6, constructed from sample accession ERS13478510 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478510">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478510</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283016" alias="SC_EXP_47423_1#426" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283016</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#426</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E10, constructed from sample accession ERS13472940 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283137" alias="SC_EXP_47423_1#547" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283137</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#547</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J17, constructed from sample accession ERS13472842 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282986" alias="SC_EXP_47423_1#396" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282986</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#396</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I2, constructed from sample accession ERS13472912 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472912">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283479" alias="SC_EXP_47433_1#212" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283479</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H15, constructed from sample accession ERS13473183 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473183">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473183</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282634" alias="SC_EXP_47408_1#724" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282634</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#724</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K2, constructed from sample accession ERS13472867 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472867">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283352" alias="SC_EXP_47433_1#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283352</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G4, constructed from sample accession ERS13478544 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478544">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478544</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381564</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283041" alias="SC_EXP_47423_1#451" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283041</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#451</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G16, constructed from sample accession ERS13472966 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283131" alias="SC_EXP_47423_1#541" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283131</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#541</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L15, constructed from sample accession ERS13472833 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472833">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472833</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283021" alias="SC_EXP_47423_1#431" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283021</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#431</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O10, constructed from sample accession ERS13472947 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283183" alias="SC_EXP_47423_1#744" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283183</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#744</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M6, constructed from sample accession ERS13472930 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472930">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472930</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283483" alias="SC_EXP_47433_1#216" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283483</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#216</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D17, constructed from sample accession ERS13473187 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473187">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376199</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283347" alias="SC_EXP_47433_1#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283347</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M2, constructed from sample accession ERS13478539 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478539">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478539</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381558</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283089" alias="SC_EXP_47423_1#499" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283089</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#499</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B5, constructed from sample accession ERS13472744 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472744">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472744</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283335" alias="SC_EXP_47423_1#897" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283335</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#897</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F23, constructed from sample accession ERS13472857 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283067" alias="SC_EXP_47423_1#477" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283067</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#477</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E24, constructed from sample accession ERS13472993 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283173" alias="SC_EXP_47423_1#734" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283173</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#734</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I4, constructed from sample accession ERS13472919 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472919">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283402" alias="SC_EXP_47433_1#135" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283402</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K16, constructed from sample accession ERS13478594 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478594">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478594</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381614</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283156" alias="SC_EXP_47423_1#566" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283156</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#566</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F23, constructed from sample accession ERS13472857 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283388" alias="SC_EXP_47433_1#121" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283388</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O12, constructed from sample accession ERS13478580 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478580">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478580</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283018" alias="SC_EXP_47423_1#428" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283018</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#428</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I10, constructed from sample accession ERS13472943 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375955</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283195" alias="SC_EXP_47423_1#756" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283195</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#756</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E10, constructed from sample accession ERS13472940 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283305" alias="SC_EXP_47423_1#866" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283305</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#866</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B15, constructed from sample accession ERS13472828 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283371" alias="SC_EXP_47433_1#104" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283371</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M8, constructed from sample accession ERS13478563 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478563">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478563</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381582</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283424" alias="SC_EXP_47433_1#157" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283424</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K22, constructed from sample accession ERS13478616 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478616">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478616</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381636</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283154" alias="SC_EXP_47423_1#564" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283154</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#564</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B23, constructed from sample accession ERS13472856 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472856">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472856</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283054" alias="SC_EXP_47423_1#464" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283054</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#464</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G20, constructed from sample accession ERS13472980 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283088" alias="SC_EXP_47423_1#498" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283088</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#498</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:P3, constructed from sample accession ERS13472746 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472746">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472746</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283193" alias="SC_EXP_47423_1#754" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283193</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#754</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A10, constructed from sample accession ERS13472941 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283405" alias="SC_EXP_47433_1#138" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283405</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A18, constructed from sample accession ERS13478598 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478598">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478598</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381617</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282833" alias="SC_EXP_47423_1#92" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282833</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M8, constructed from sample accession ERS13472937 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472937">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283102" alias="SC_EXP_47423_1#512" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283102</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#512</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L7, constructed from sample accession ERS13472804 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472804">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282414" alias="SC_EXP_47408_1#290" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282414</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#290</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D14, constructed from sample accession ERS13473021 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283495" alias="SC_EXP_47433_1#228" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283495</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#228</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D21, constructed from sample accession ERS13473199 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473199">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473199</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282685" alias="SC_EXP_47408_1#775" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282685</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#775</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A16, constructed from sample accession ERS13472793 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472793">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283380" alias="SC_EXP_47433_1#113" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283380</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O10, constructed from sample accession ERS13478572 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478572">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478572</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283372" alias="SC_EXP_47433_1#105" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283372</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O8, constructed from sample accession ERS13478564 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478564">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478564</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381583</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282349" alias="SC_EXP_47408_1#131" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282349</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#131</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M18, constructed from sample accession ERS13472888 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472888">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472888</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283408" alias="SC_EXP_47433_1#141" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283408</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G18, constructed from sample accession ERS13478600 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478600">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478600</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381620</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283009" alias="SC_EXP_47423_1#419" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283009</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#419</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G8, constructed from sample accession ERS13472932 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472932">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472932</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283076" alias="SC_EXP_47423_1#486" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283076</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#486</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H1, constructed from sample accession ERS13472732 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472732">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472732</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282840" alias="SC_EXP_47423_1#99" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282840</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K10, constructed from sample accession ERS13472944 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283525" alias="SC_EXP_47433_1#258" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283525</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#258</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L6, constructed from sample accession ERS13478511 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478511">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478511</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381531</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283314" alias="SC_EXP_47423_1#875" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283314</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#875</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F17, constructed from sample accession ERS13472837 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472837">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472837</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282695" alias="SC_EXP_47408_1#785" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282695</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#785</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E18, constructed from sample accession ERS13472884 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283243" alias="SC_EXP_47423_1#804" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283243</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#804</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M22, constructed from sample accession ERS13472990 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472990">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282967" alias="SC_EXP_47423_1#226" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282967</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#226</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N19, constructed from sample accession ERS13472848 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282569" alias="SC_EXP_47408_1#599" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282569</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#599</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F8, constructed from sample accession ERS13473130 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282937" alias="SC_EXP_47423_1#196" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282937</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J11, constructed from sample accession ERS13472818 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472818">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472818</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283508" alias="SC_EXP_47433_1#241" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283508</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#241</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F2, constructed from sample accession ERS13478493 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478493">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381513</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282916" alias="SC_EXP_47423_1#175" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282916</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#175</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N5, constructed from sample accession ERS13472796 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472796">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283471" alias="SC_EXP_47433_1#204" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283471</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#204</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D13, constructed from sample accession ERS13473175 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473175">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376187</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283065" alias="SC_EXP_47423_1#475" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283065</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#475</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A24, constructed from sample accession ERS13472992 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472992">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472992</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282528" alias="SC_EXP_47408_1#464" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282528</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#464</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I20, constructed from sample accession ERS13472892 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472892">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472892</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282876" alias="SC_EXP_47423_1#135" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282876</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#135</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I20, constructed from sample accession ERS13472981 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472981">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282369" alias="SC_EXP_47408_1#151" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282369</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#151</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M24, constructed from sample accession ERS13472908 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283318" alias="SC_EXP_47423_1#879" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283318</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#879</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N17, constructed from sample accession ERS13472840 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472840">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472840</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283224" alias="SC_EXP_47423_1#785" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283224</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#785</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O16, constructed from sample accession ERS13472971 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283369" alias="SC_EXP_47433_1#102" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283369</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I8, constructed from sample accession ERS13478561 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478561">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478561</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381581</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283297" alias="SC_EXP_47423_1#858" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283297</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#858</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N11, constructed from sample accession ERS13472820 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472820">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472820</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282430" alias="SC_EXP_47408_1#306" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282430</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H18, constructed from sample accession ERS13473036 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282565" alias="SC_EXP_47408_1#595" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282565</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#595</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L6, constructed from sample accession ERS13473126 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473126">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473126</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282415" alias="SC_EXP_47408_1#291" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282415</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#291</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F14, constructed from sample accession ERS13473020 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473020">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473020</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283486" alias="SC_EXP_47433_1#219" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283486</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#219</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J17, constructed from sample accession ERS13473190 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473190">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473190</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282527" alias="SC_EXP_47408_1#463" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282527</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#463</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G20, constructed from sample accession ERS13472891 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472891">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472891</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282303" alias="SC_EXP_47408_1#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282303</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A8, constructed from sample accession ERS13472766 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472766">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472766</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283420" alias="SC_EXP_47433_1#153" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283420</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C22, constructed from sample accession ERS13478612 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478612">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478612</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381632</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282487" alias="SC_EXP_47408_1#423" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282487</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#423</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C10, constructed from sample accession ERS13472775 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472775">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283121" alias="SC_EXP_47423_1#531" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283121</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#531</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F13, constructed from sample accession ERS13472822 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472822">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472822</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283246" alias="SC_EXP_47423_1#807" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283246</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#807</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E24, constructed from sample accession ERS13472993 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283159" alias="SC_EXP_47423_1#569" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283159</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#569</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L23, constructed from sample accession ERS13472859 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472859">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282661" alias="SC_EXP_47408_1#751" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282661</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#751</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A10, constructed from sample accession ERS13472771 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472771">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283386" alias="SC_EXP_47433_1#119" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283386</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K12, constructed from sample accession ERS13478579 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478579">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478579</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282418" alias="SC_EXP_47408_1#294" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282418</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L14, constructed from sample accession ERS13473024 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283013" alias="SC_EXP_47423_1#423" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283013</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#423</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O8, constructed from sample accession ERS13472946 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282853" alias="SC_EXP_47423_1#112" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282853</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E14, constructed from sample accession ERS13472957 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472957">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472957</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283206" alias="SC_EXP_47423_1#767" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283206</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#767</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K12, constructed from sample accession ERS13472953 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283473" alias="SC_EXP_47433_1#206" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283473</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H13, constructed from sample accession ERS13473177 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473177">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282680" alias="SC_EXP_47408_1#770" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282680</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#770</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G14, constructed from sample accession ERS13472789 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472789">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472789</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283414" alias="SC_EXP_47433_1#147" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283414</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E20, constructed from sample accession ERS13478606 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478606">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478606</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381626</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282936" alias="SC_EXP_47423_1#195" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282936</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H11, constructed from sample accession ERS13472817 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472817">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283330" alias="SC_EXP_47423_1#892" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283330</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#892</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J21, constructed from sample accession ERS13472853 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472853">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472853</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282641" alias="SC_EXP_47408_1#731" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282641</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#731</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I4, constructed from sample accession ERS13472875 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472875">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283400" alias="SC_EXP_47433_1#133" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283400</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#133</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G16, constructed from sample accession ERS13478591 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478591">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478591</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282392" alias="SC_EXP_47408_1#268" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282392</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#268</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B8, constructed from sample accession ERS13473129 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473129">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473129</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282604" alias="SC_EXP_47408_1#634" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282604</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#634</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F18, constructed from sample accession ERS13473035 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473035">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473035</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283448" alias="SC_EXP_47433_1#181" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283448</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F5, constructed from sample accession ERS13473152 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473152">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282933" alias="SC_EXP_47423_1#192" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282933</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B11, constructed from sample accession ERS13472814 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283215" alias="SC_EXP_47423_1#776" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283215</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#776</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M14, constructed from sample accession ERS13472964 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282328" alias="SC_EXP_47408_1#110" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282328</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C14, constructed from sample accession ERS13472787 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472787">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282495" alias="SC_EXP_47408_1#431" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282495</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#431</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C12, constructed from sample accession ERS13472779 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472779">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282930" alias="SC_EXP_47423_1#189" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282930</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#189</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J9, constructed from sample accession ERS13472811 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472811">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282815" alias="SC_EXP_47423_1#74" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282815</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I4, constructed from sample accession ERS13472919 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472919">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283199" alias="SC_EXP_47423_1#760" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283199</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#760</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M10, constructed from sample accession ERS13472945 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375957</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282750" alias="SC_EXP_47408_1#935" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282750</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#935</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D10, constructed from sample accession ERS13473137 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282985" alias="SC_EXP_47423_1#395" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282985</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#395</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G2, constructed from sample accession ERS13472910 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472910">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282847" alias="SC_EXP_47423_1#106" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282847</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I12, constructed from sample accession ERS13472952 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283321" alias="SC_EXP_47423_1#882" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283321</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#882</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F19, constructed from sample accession ERS13472844 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472844">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472844</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282834" alias="SC_EXP_47423_1#93" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282834</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#93</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O8, constructed from sample accession ERS13472946 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375958</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282765" alias="SC_EXP_47408_1#950" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282765</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#950</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F14, constructed from sample accession ERS13473020 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473020">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473020</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376032</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282455" alias="SC_EXP_47408_1#391" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282455</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#391</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C2, constructed from sample accession ERS13472864 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472864">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472864</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282436" alias="SC_EXP_47408_1#312" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282436</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F20, constructed from sample accession ERS13473042 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAATCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376054</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283312" alias="SC_EXP_47423_1#873" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283312</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#873</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B17, constructed from sample accession ERS13472835 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472835">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472835</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282781" alias="SC_EXP_47408_1#966" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282781</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#966</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J18, constructed from sample accession ERS13473037 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473037">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283382" alias="SC_EXP_47433_1#115" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283382</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#115</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C12, constructed from sample accession ERS13478573 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478573">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478573</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381593</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282356" alias="SC_EXP_47408_1#138" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282356</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#138</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A22, constructed from sample accession ERS13472896 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472896">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472896</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283283" alias="SC_EXP_47423_1#844" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283283</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#844</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:P7, constructed from sample accession ERS13472805 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472805">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:P7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282681" alias="SC_EXP_47408_1#771" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282681</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#771</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I14, constructed from sample accession ERS13472790 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472790">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282381" alias="SC_EXP_47408_1#257" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282381</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#257</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H4, constructed from sample accession ERS13473117 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283234" alias="SC_EXP_47423_1#795" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283234</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#795</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I20, constructed from sample accession ERS13472981 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472981">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283368" alias="SC_EXP_47433_1#101" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283368</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G8, constructed from sample accession ERS13478560 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478560">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478560</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381580</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283306" alias="SC_EXP_47423_1#867" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283306</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#867</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:D15, constructed from sample accession ERS13472829 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472829">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472829</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:D15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283134" alias="SC_EXP_47423_1#544" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283134</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#544</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D17, constructed from sample accession ERS13472836 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472836">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283459" alias="SC_EXP_47433_1#192" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283459</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#192</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D9, constructed from sample accession ERS13473163 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473163">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283263" alias="SC_EXP_47423_1#824" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283263</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#824</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H3, constructed from sample accession ERS13472741 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472741">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472741</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282413" alias="SC_EXP_47408_1#289" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282413</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#289</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B14, constructed from sample accession ERS13473019 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473019">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473019</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376031</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282900" alias="SC_EXP_47423_1#159" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282900</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N1, constructed from sample accession ERS13472736 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472736">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472736</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282894" alias="SC_EXP_47423_1#153" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282894</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#153</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B1, constructed from sample accession ERS13472730 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472730">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472730</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283469" alias="SC_EXP_47433_1#202" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283469</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#202</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L11, constructed from sample accession ERS13473172 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473172">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376185</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283433" alias="SC_EXP_47433_1#166" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283433</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#166</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O24, constructed from sample accession ERS15458434 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15458434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15458434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113462668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282843" alias="SC_EXP_47423_1#102" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282843</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A12, constructed from sample accession ERS13472948 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282819" alias="SC_EXP_47423_1#78" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282819</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#78</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A6, constructed from sample accession ERS13472922 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472922">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283276" alias="SC_EXP_47423_1#837" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283276</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#837</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B7, constructed from sample accession ERS13472798 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472798">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282496" alias="SC_EXP_47408_1#432" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282496</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#432</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E12, constructed from sample accession ERS13472781 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472781">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283118" alias="SC_EXP_47423_1#528" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283118</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#528</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N11, constructed from sample accession ERS13472820 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472820">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472820</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282704" alias="SC_EXP_47408_1#794" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282704</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#794</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K20, constructed from sample accession ERS13472894 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472894">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282981" alias="SC_EXP_47423_1#240" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282981</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N23, constructed from sample accession ERS13472862 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472862">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283461" alias="SC_EXP_47433_1#194" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283461</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H9, constructed from sample accession ERS13473167 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473167">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283489" alias="SC_EXP_47433_1#222" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283489</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#222</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D19, constructed from sample accession ERS13473193 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473193">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473193</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376205</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282316" alias="SC_EXP_47408_1#98" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282316</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#98</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K10, constructed from sample accession ERS13472776 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472776">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472776</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282338" alias="SC_EXP_47408_1#120" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282338</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#120</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G16, constructed from sample accession ERS13472877 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472877">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283462" alias="SC_EXP_47433_1#195" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283462</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#195</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J9, constructed from sample accession ERS13473166 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473166">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473166</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283376" alias="SC_EXP_47433_1#109" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283376</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G10, constructed from sample accession ERS13478567 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478567">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478567</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381587</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283194" alias="SC_EXP_47423_1#755" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283194</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#755</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C10, constructed from sample accession ERS13472939 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472939">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282882" alias="SC_EXP_47423_1#141" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282882</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G22, constructed from sample accession ERS13472986 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283273" alias="SC_EXP_47423_1#834" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283273</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#834</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L5, constructed from sample accession ERS13472750 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472750">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472750</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282416" alias="SC_EXP_47408_1#292" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282416</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#292</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H14, constructed from sample accession ERS13473022 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473022">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282298" alias="SC_EXP_47408_1#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282298</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G6, constructed from sample accession ERS13472758 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472758">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472758</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375769</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283349" alias="SC_EXP_47433_1#82" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283349</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#82</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A4, constructed from sample accession ERS13478541 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478541">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478541</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381561</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283190" alias="SC_EXP_47423_1#751" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283190</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#751</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:K8, constructed from sample accession ERS13472936 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472936">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472936</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282562" alias="SC_EXP_47408_1#592" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282562</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#592</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F6, constructed from sample accession ERS13473127 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282480" alias="SC_EXP_47408_1#416" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282480</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#416</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E8, constructed from sample accession ERS13472764 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472764">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472764</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282297" alias="SC_EXP_47408_1#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282297</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E6, constructed from sample accession ERS13472757 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472757">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282612" alias="SC_EXP_47408_1#642" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282612</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#642</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H20, constructed from sample accession ERS13473043 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282974" alias="SC_EXP_47423_1#233" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282974</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N21, constructed from sample accession ERS13472855 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472855">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472855</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282324" alias="SC_EXP_47408_1#106" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282324</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K12, constructed from sample accession ERS13472784 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472784">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282635" alias="SC_EXP_47408_1#725" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282635</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#725</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M2, constructed from sample accession ERS13472872 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472872">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282592" alias="SC_EXP_47408_1#622" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282592</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#622</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J14, constructed from sample accession ERS13473023 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473023">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473023</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282558" alias="SC_EXP_47408_1#588" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282558</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#588</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L4, constructed from sample accession ERS13473118 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282402" alias="SC_EXP_47408_1#278" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282402</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#278</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H10, constructed from sample accession ERS13473008 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376021</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282423" alias="SC_EXP_47408_1#299" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282423</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H16, constructed from sample accession ERS13473028 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473028">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282844" alias="SC_EXP_47423_1#103" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282844</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C12, constructed from sample accession ERS13472949 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282932" alias="SC_EXP_47423_1#191" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282932</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N9, constructed from sample accession ERS13472813 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472813">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472813</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282557" alias="SC_EXP_47408_1#587" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282557</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#587</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J4, constructed from sample accession ERS13473123 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282393" alias="SC_EXP_47408_1#269" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282393</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#269</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D8, constructed from sample accession ERS13473133 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473133">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282312" alias="SC_EXP_47408_1#94" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282312</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C10, constructed from sample accession ERS13472775 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472775">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282626" alias="SC_EXP_47408_1#656" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282626</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L24, constructed from sample accession ERS13473057 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282492" alias="SC_EXP_47408_1#428" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282492</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#428</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M10, constructed from sample accession ERS13472777 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472777">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282810" alias="SC_EXP_47423_1#69" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282810</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#69</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O2, constructed from sample accession ERS13472915 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472915">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282613" alias="SC_EXP_47408_1#643" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282613</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#643</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J20, constructed from sample accession ERS13473044 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473044">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473044</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283074" alias="SC_EXP_47423_1#484" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283074</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#484</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D1, constructed from sample accession ERS13472733 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472733">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472733</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282563" alias="SC_EXP_47408_1#593" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282563</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#593</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H6, constructed from sample accession ERS13473124 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473124">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473124</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282341" alias="SC_EXP_47408_1#123" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282341</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M16, constructed from sample accession ERS13472880 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472880">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283039" alias="SC_EXP_47423_1#449" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283039</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#449</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C16, constructed from sample accession ERS13472965 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282700" alias="SC_EXP_47408_1#790" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282700</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#790</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A20, constructed from sample accession ERS13472889 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283038" alias="SC_EXP_47423_1#448" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283038</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#448</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A16, constructed from sample accession ERS13472963 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283010" alias="SC_EXP_47423_1#420" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283010</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#420</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I8, constructed from sample accession ERS13472935 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472935">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472935</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283487" alias="SC_EXP_47433_1#220" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283487</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#220</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L17, constructed from sample accession ERS13473192 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473192">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473192</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376204</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282394" alias="SC_EXP_47408_1#270" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282394</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#270</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F8, constructed from sample accession ERS13473130 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282769" alias="SC_EXP_47408_1#954" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282769</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#954</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:N14, constructed from sample accession ERS13473026 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473026">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:N14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283391" alias="SC_EXP_47433_1#124" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283391</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:E14, constructed from sample accession ERS13478583 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478583">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478583</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282860" alias="SC_EXP_47423_1#119" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282860</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#119</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C16, constructed from sample accession ERS13472965 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283098" alias="SC_EXP_47423_1#508" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283098</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#508</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D7, constructed from sample accession ERS13472799 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472799">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282566" alias="SC_EXP_47408_1#596" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282566</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#596</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N6, constructed from sample accession ERS13473128 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282804" alias="SC_EXP_47423_1#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282804</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A2, constructed from sample accession ERS13472909 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472909">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472909</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282577" alias="SC_EXP_47408_1#607" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282577</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#607</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H10, constructed from sample accession ERS13473008 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376021</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283507" alias="SC_EXP_47433_1#240" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283507</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#240</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D2, constructed from sample accession ERS13478500 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478500">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478500</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381520</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282954" alias="SC_EXP_47423_1#213" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282954</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#213</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B17, constructed from sample accession ERS13472835 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472835">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472835</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283422" alias="SC_EXP_47433_1#155" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283422</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G22, constructed from sample accession ERS13478614 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478614">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478614</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381634</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282600" alias="SC_EXP_47408_1#630" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282600</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#630</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L16, constructed from sample accession ERS13473030 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282938" alias="SC_EXP_47423_1#197" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282938</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L11, constructed from sample accession ERS13472819 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472819">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282643" alias="SC_EXP_47408_1#733" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282643</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#733</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M4, constructed from sample accession ERS13472753 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472753">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472753</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282534" alias="SC_EXP_47408_1#470" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282534</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#470</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G22, constructed from sample accession ERS13472899 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472899">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283523" alias="SC_EXP_47433_1#256" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283523</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#256</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H6, constructed from sample accession ERS13478509 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478509">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478509</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282941" alias="SC_EXP_47423_1#200" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282941</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D13, constructed from sample accession ERS13472821 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472821">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472821</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282593" alias="SC_EXP_47408_1#623" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282593</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#623</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L14, constructed from sample accession ERS13473024 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282671" alias="SC_EXP_47408_1#761" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282671</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#761</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E12, constructed from sample accession ERS13472781 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472781">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282947" alias="SC_EXP_47423_1#206" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282947</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#206</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B15, constructed from sample accession ERS13472828 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282551" alias="SC_EXP_47408_1#581" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282551</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#581</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L2, constructed from sample accession ERS13473113 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283152" alias="SC_EXP_47423_1#562" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283152</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#562</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L21, constructed from sample accession ERS13472854 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282935" alias="SC_EXP_47423_1#194" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282935</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#194</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F11, constructed from sample accession ERS13472816 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472816">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283070" alias="SC_EXP_47423_1#480" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283070</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#480</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K24, constructed from sample accession ERS13472996 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472996">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472996</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283160" alias="SC_EXP_47423_1#570" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283160</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#570</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N23, constructed from sample accession ERS13472862 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472862">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472862</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282864" alias="SC_EXP_47423_1#123" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282864</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#123</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K16, constructed from sample accession ERS13472968 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283051" alias="SC_EXP_47423_1#461" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283051</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#461</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K18, constructed from sample accession ERS13472977 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283081" alias="SC_EXP_47423_1#491" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283081</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#491</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B3, constructed from sample accession ERS13472738 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472738">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472738</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283233" alias="SC_EXP_47423_1#794" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283233</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#794</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G20, constructed from sample accession ERS13472980 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283046" alias="SC_EXP_47423_1#456" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283046</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#456</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A18, constructed from sample accession ERS13472972 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472972">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282585" alias="SC_EXP_47408_1#615" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282585</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#615</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J12, constructed from sample accession ERS13473015 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282540" alias="SC_EXP_47408_1#476" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282540</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#476</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E24, constructed from sample accession ERS13472906 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472906">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472906</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282489" alias="SC_EXP_47408_1#425" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282489</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#425</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:G10, constructed from sample accession ERS13472773 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472773">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472773</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282304" alias="SC_EXP_47408_1#86" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282304</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C8, constructed from sample accession ERS13472763 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472763">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472763</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282442" alias="SC_EXP_47408_1#318" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282442</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#318</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F22, constructed from sample accession ERS13473048 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473048">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283130" alias="SC_EXP_47423_1#540" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283130</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#540</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J15, constructed from sample accession ERS13472832 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472832">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283384" alias="SC_EXP_47433_1#117" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283384</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G12, constructed from sample accession ERS13478577 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478577">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478577</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283500" alias="SC_EXP_47433_1#233" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283500</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#233</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D23, constructed from sample accession ERS13473204 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473204">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473204</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282987" alias="SC_EXP_47423_1#397" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282987</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#397</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K2, constructed from sample accession ERS13472913 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472913">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283255" alias="SC_EXP_47423_1#816" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283255</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#816</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H1, constructed from sample accession ERS13472732 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472732">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472732</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283022" alias="SC_EXP_47423_1#432" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283022</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#432</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A12, constructed from sample accession ERS13472948 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282914" alias="SC_EXP_47423_1#173" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282914</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J5, constructed from sample accession ERS13472748 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472748">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283082" alias="SC_EXP_47423_1#492" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283082</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#492</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D3, constructed from sample accession ERS13472739 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472739">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472739</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283147" alias="SC_EXP_47423_1#557" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283147</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#557</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B21, constructed from sample accession ERS13472849 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472849">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472849</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283458" alias="SC_EXP_47433_1#191" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283458</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#191</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B9, constructed from sample accession ERS13473162 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473162">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473162</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282478" alias="SC_EXP_47408_1#414" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282478</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#414</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A8, constructed from sample accession ERS13472766 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472766">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472766</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282281" alias="SC_EXP_47408_1#63" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282281</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E2, constructed from sample accession ERS13472865 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472865">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472865</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282909" alias="SC_EXP_47423_1#168" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282909</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:P3, constructed from sample accession ERS13472746 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472746">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472746</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283355" alias="SC_EXP_47433_1#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283355</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M4, constructed from sample accession ERS13478547 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478547">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478547</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283301" alias="SC_EXP_47423_1#862" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283301</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#862</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H13, constructed from sample accession ERS13472823 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472823">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472823</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283024" alias="SC_EXP_47423_1#434" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283024</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#434</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E12, constructed from sample accession ERS13472950 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282648" alias="SC_EXP_47408_1#738" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282648</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#738</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G6, constructed from sample accession ERS13472758 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472758">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472758</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375769</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282568" alias="SC_EXP_47408_1#598" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282568</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#598</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D8, constructed from sample accession ERS13473133 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473133">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282713" alias="SC_EXP_47408_1#803" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282713</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#803</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A24, constructed from sample accession ERS13472900 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472900">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283304" alias="SC_EXP_47423_1#865" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283304</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#865</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:N13, constructed from sample accession ERS13472827 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472827">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472827</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:N13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283167" alias="SC_EXP_47423_1#728" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283167</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#728</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:M2, constructed from sample accession ERS13472914 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:M2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282980" alias="SC_EXP_47423_1#239" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282980</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L23, constructed from sample accession ERS13472859 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472859">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472859</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283472" alias="SC_EXP_47433_1#205" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283472</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#205</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F13, constructed from sample accession ERS13473176 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473176">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376188</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282448" alias="SC_EXP_47408_1#324" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282448</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F24, constructed from sample accession ERS13473053 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283027" alias="SC_EXP_47423_1#437" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283027</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#437</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K12, constructed from sample accession ERS13472953 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283172" alias="SC_EXP_47423_1#733" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283172</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#733</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G4, constructed from sample accession ERS13472918 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472918">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282522" alias="SC_EXP_47408_1#458" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282522</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#458</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I18, constructed from sample accession ERS13472886 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282689" alias="SC_EXP_47408_1#779" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282689</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#779</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I16, constructed from sample accession ERS13472878 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472878">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283522" alias="SC_EXP_47433_1#255" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283522</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#255</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F6, constructed from sample accession ERS13478508 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478508">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478508</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282994" alias="SC_EXP_47423_1#404" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282994</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#404</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I4, constructed from sample accession ERS13472919 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472919">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282820" alias="SC_EXP_47423_1#79" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282820</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C6, constructed from sample accession ERS13472925 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283357" alias="SC_EXP_47433_1#90" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283357</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#90</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A6, constructed from sample accession ERS13478549 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478549">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478549</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282984" alias="SC_EXP_47423_1#394" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282984</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#394</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C2, constructed from sample accession ERS13472911 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282760" alias="SC_EXP_47408_1#945" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282760</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#945</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J12, constructed from sample accession ERS13473015 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376027</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282411" alias="SC_EXP_47408_1#287" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282411</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#287</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L12, constructed from sample accession ERS13473017 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473017">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473017</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376029</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282720" alias="SC_EXP_47408_1#810" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282720</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#810</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O24, constructed from sample accession ERS15395411 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282598" alias="SC_EXP_47408_1#628" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282598</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#628</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H16, constructed from sample accession ERS13473028 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473028">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282572" alias="SC_EXP_47408_1#602" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282572</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#602</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L8, constructed from sample accession ERS13473134 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283260" alias="SC_EXP_47423_1#821" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283260</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#821</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B3, constructed from sample accession ERS13472738 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472738">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472738</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282617" alias="SC_EXP_47408_1#647" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282617</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#647</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F22, constructed from sample accession ERS13473048 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473048">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282408" alias="SC_EXP_47408_1#284" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282408</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#284</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F12, constructed from sample accession ERS13473013 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473013">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283145" alias="SC_EXP_47423_1#555" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283145</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#555</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L19, constructed from sample accession ERS13472847 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472847">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472847</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283092" alias="SC_EXP_47423_1#502" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283092</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#502</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H5, constructed from sample accession ERS13472747 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472747">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472747</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283454" alias="SC_EXP_47433_1#187" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283454</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#187</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F7, constructed from sample accession ERS13473158 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473158">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282549" alias="SC_EXP_47408_1#579" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282549</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#579</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H2, constructed from sample accession ERS13473110 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473110">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473110</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283497" alias="SC_EXP_47433_1#230" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283497</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#230</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H21, constructed from sample accession ERS13473201 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473201">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473201</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283045" alias="SC_EXP_47423_1#455" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283045</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#455</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O16, constructed from sample accession ERS13472971 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283002" alias="SC_EXP_47423_1#412" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283002</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#412</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I6, constructed from sample accession ERS13472927 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472927">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472927</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282628" alias="SC_EXP_47408_1#658" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282628</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#658</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:P24, constructed from sample accession ERS15395416 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:P24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282607" alias="SC_EXP_47408_1#637" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282607</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#637</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L18, constructed from sample accession ERS13473038 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473038">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473038</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283513" alias="SC_EXP_47433_1#246" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283513</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#246</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B4, constructed from sample accession ERS13478498 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478498">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478498</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381518</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282618" alias="SC_EXP_47408_1#648" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282618</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#648</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:H22, constructed from sample accession ERS13473049 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:H22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282824" alias="SC_EXP_47423_1#83" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282824</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#83</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K6, constructed from sample accession ERS13472926 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472926">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472926</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283464" alias="SC_EXP_47433_1#197" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283464</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#197</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B11, constructed from sample accession ERS13473170 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473170">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283257" alias="SC_EXP_47423_1#818" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283257</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#818</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L1, constructed from sample accession ERS13472735 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472735">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472735</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282915" alias="SC_EXP_47423_1#174" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282915</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#174</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L5, constructed from sample accession ERS13472750 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472750">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472750</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283015" alias="SC_EXP_47423_1#425" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283015</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#425</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C10, constructed from sample accession ERS13472939 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472939">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375951</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282993" alias="SC_EXP_47423_1#403" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282993</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#403</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G4, constructed from sample accession ERS13472918 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472918">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282343" alias="SC_EXP_47408_1#125" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282343</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#125</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A18, constructed from sample accession ERS13472882 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472882">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472882</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283136" alias="SC_EXP_47423_1#546" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283136</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#546</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H17, constructed from sample accession ERS13472838 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472838">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282773" alias="SC_EXP_47408_1#958" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282773</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#958</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H16, constructed from sample accession ERS13473028 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473028">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473028</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283073" alias="SC_EXP_47423_1#483" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283073</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#483</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B1, constructed from sample accession ERS13472730 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472730">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472730</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282653" alias="SC_EXP_47408_1#743" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282653</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#743</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A8, constructed from sample accession ERS13472766 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472766">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472766</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283033" alias="SC_EXP_47423_1#443" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283033</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#443</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G14, constructed from sample accession ERS13472958 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282525" alias="SC_EXP_47408_1#461" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282525</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#461</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A20, constructed from sample accession ERS13472889 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283515" alias="SC_EXP_47433_1#248" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283515</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#248</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F4, constructed from sample accession ERS13478499 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478499">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478499</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381519</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282326" alias="SC_EXP_47408_1#108" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282326</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O12, constructed from sample accession ERS13472786 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472786">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282646" alias="SC_EXP_47408_1#736" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282646</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#736</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C6, constructed from sample accession ERS13472756 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472756">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472756</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282955" alias="SC_EXP_47423_1#214" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282955</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#214</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D17, constructed from sample accession ERS13472836 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472836">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282581" alias="SC_EXP_47408_1#611" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282581</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#611</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B12, constructed from sample accession ERS13473012 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473012">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473012</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282350" alias="SC_EXP_47408_1#132" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282350</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#132</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A20, constructed from sample accession ERS13472889 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282716" alias="SC_EXP_47408_1#806" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282716</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#806</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G24, constructed from sample accession ERS13472903 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472903">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472903</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282731" alias="SC_EXP_47408_1#916" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282731</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#916</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H4, constructed from sample accession ERS13473117 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283003" alias="SC_EXP_47423_1#413" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283003</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#413</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K6, constructed from sample accession ERS13472926 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472926">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472926</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282813" alias="SC_EXP_47423_1#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282813</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E4, constructed from sample accession ERS13472917 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282358" alias="SC_EXP_47408_1#140" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282358</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#140</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E22, constructed from sample accession ERS13472897 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472897">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282973" alias="SC_EXP_47423_1#232" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282973</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#232</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L21, constructed from sample accession ERS13472854 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282479" alias="SC_EXP_47408_1#415" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282479</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#415</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C8, constructed from sample accession ERS13472763 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472763">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472763</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282283" alias="SC_EXP_47408_1#65" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282283</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I2, constructed from sample accession ERS13472868 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472868">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282953" alias="SC_EXP_47423_1#212" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282953</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#212</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N15, constructed from sample accession ERS13472834 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472834">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282649" alias="SC_EXP_47408_1#739" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282649</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#739</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I6, constructed from sample accession ERS13472759 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472759">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472759</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283506" alias="SC_EXP_47433_1#239" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283506</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#239</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B2, constructed from sample accession ERS13478492 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478492">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478492</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381512</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282905" alias="SC_EXP_47423_1#164" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282905</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#164</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H3, constructed from sample accession ERS13472741 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472741">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472741</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282589" alias="SC_EXP_47408_1#619" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282589</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#619</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D14, constructed from sample accession ERS13473021 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282829" alias="SC_EXP_47423_1#88" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282829</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E8, constructed from sample accession ERS13472934 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282639" alias="SC_EXP_47408_1#729" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282639</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#729</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E4, constructed from sample accession ERS13472873 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472873">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283512" alias="SC_EXP_47433_1#245" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283512</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#245</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:N2, constructed from sample accession ERS13478497 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478497">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478497</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381517</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:N2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283066" alias="SC_EXP_47423_1#476" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283066</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#476</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:C24, constructed from sample accession ERS13472991 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282737" alias="SC_EXP_47408_1#922" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282737</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#922</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F6, constructed from sample accession ERS13473127 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473127">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473127</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282435" alias="SC_EXP_47408_1#311" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282435</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:D20, constructed from sample accession ERS13473041 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473041">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:D20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282673" alias="SC_EXP_47408_1#763" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282673</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#763</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I12, constructed from sample accession ERS13472783 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472783">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282862" alias="SC_EXP_47423_1#121" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282862</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#121</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G16, constructed from sample accession ERS13472966 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282403" alias="SC_EXP_47408_1#279" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282403</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#279</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J10, constructed from sample accession ERS13473009 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473009">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473009</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376020</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283501" alias="SC_EXP_47433_1#234" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283501</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#234</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F23, constructed from sample accession ERS13473205 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473205">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473205</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282706" alias="SC_EXP_47408_1#796" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282706</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#796</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:A22, constructed from sample accession ERS13472896 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472896">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472896</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282679" alias="SC_EXP_47408_1#769" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282679</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#769</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E14, constructed from sample accession ERS13472792 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472792">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472792</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283116" alias="SC_EXP_47423_1#526" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283116</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#526</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J11, constructed from sample accession ERS13472818 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472818">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472818</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282354" alias="SC_EXP_47408_1#136" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282354</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K20, constructed from sample accession ERS13472894 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472894">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472894</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282282" alias="SC_EXP_47408_1#64" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282282</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G2, constructed from sample accession ERS13472866 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283278" alias="SC_EXP_47423_1#839" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283278</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#839</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F7, constructed from sample accession ERS13472800 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472800">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472800</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282537" alias="SC_EXP_47408_1#473" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282537</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#473</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M22, constructed from sample accession ERS13472904 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472904">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283498" alias="SC_EXP_47433_1#231" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283498</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#231</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J21, constructed from sample accession ERS13473202 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473202">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473202</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376214</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282676" alias="SC_EXP_47408_1#766" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282676</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#766</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:O12, constructed from sample accession ERS13472786 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472786">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283201" alias="SC_EXP_47423_1#762" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283201</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#762</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A12, constructed from sample accession ERS13472948 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282785" alias="SC_EXP_47408_1#970" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282785</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#970</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D20, constructed from sample accession ERS13473041 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTCGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473041">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473041</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283403" alias="SC_EXP_47433_1#136" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283403</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:M16, constructed from sample accession ERS13478595 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478595">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478595</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381615</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282398" alias="SC_EXP_47408_1#274" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282398</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#274</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N8, constructed from sample accession ERS13473135 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283204" alias="SC_EXP_47423_1#765" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283204</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#765</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G12, constructed from sample accession ERS13472951 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282531" alias="SC_EXP_47408_1#467" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282531</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#467</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A22, constructed from sample accession ERS13472896 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472896">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472896</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283146" alias="SC_EXP_47423_1#556" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283146</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#556</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N19, constructed from sample accession ERS13472848 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283078" alias="SC_EXP_47423_1#488" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283078</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#488</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:L1, constructed from sample accession ERS13472735 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472735">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472735</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283444" alias="SC_EXP_47433_1#177" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283444</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#177</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:J3, constructed from sample accession ERS13473148 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473148">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:J3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283323" alias="SC_EXP_47423_1#884" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283323</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#884</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J19, constructed from sample accession ERS13472846 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472846">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472846</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282697" alias="SC_EXP_47408_1#787" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282697</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#787</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I18, constructed from sample accession ERS13472886 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282391" alias="SC_EXP_47408_1#267" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282391</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#267</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N6, constructed from sample accession ERS13473128 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473128">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473128</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282658" alias="SC_EXP_47408_1#748" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282658</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#748</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K8, constructed from sample accession ERS13472768 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472768">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282493" alias="SC_EXP_47408_1#429" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282493</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#429</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O10, constructed from sample accession ERS13472778 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472778">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282627" alias="SC_EXP_47408_1#657" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282627</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#657</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N24, constructed from sample accession ERS15395415 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400268</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282323" alias="SC_EXP_47408_1#105" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282323</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I12, constructed from sample accession ERS13472783 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472783">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282688" alias="SC_EXP_47408_1#778" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282688</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#778</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:G16, constructed from sample accession ERS13472877 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472877">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:G16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282458" alias="SC_EXP_47408_1#394" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282458</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#394</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:I2, constructed from sample accession ERS13472868 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472868">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:I2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282499" alias="SC_EXP_47408_1#435" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282499</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#435</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K12, constructed from sample accession ERS13472784 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472784">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282650" alias="SC_EXP_47408_1#740" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282650</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#740</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K6, constructed from sample accession ERS13472762 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472762">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472762</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282890" alias="SC_EXP_47423_1#149" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282890</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#149</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I24, constructed from sample accession ERS13472995 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282884" alias="SC_EXP_47423_1#143" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282884</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K22, constructed from sample accession ERS13472988 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282921" alias="SC_EXP_47423_1#180" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282921</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#180</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H7, constructed from sample accession ERS13472801 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472801">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282321" alias="SC_EXP_47408_1#103" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282321</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E12, constructed from sample accession ERS13472781 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472781">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282888" alias="SC_EXP_47423_1#147" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282888</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#147</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E24, constructed from sample accession ERS13472993 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GACCTTAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283378" alias="SC_EXP_47433_1#111" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283378</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K10, constructed from sample accession ERS13478570 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478570">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478570</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381590</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282842" alias="SC_EXP_47423_1#101" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282842</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O10, constructed from sample accession ERS13472947 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282949" alias="SC_EXP_47423_1#208" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282949</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#208</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F15, constructed from sample accession ERS13472830 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472830">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282431" alias="SC_EXP_47408_1#307" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282431</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J18, constructed from sample accession ERS13473037 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473037">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473037</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282732" alias="SC_EXP_47408_1#917" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282732</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#917</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J4, constructed from sample accession ERS13473123 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283435" alias="SC_EXP_47433_1#168" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283435</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#168</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:D1, constructed from sample accession ERS13473139 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473139">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283025" alias="SC_EXP_47423_1#435" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283025</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#435</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G12, constructed from sample accession ERS13472951 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282799" alias="SC_EXP_47408_1#984" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282799</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#984</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H24, constructed from sample accession ERS13473054 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473054">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282657" alias="SC_EXP_47408_1#747" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282657</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#747</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:I8, constructed from sample accession ERS13472767 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472767">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472767</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:I8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282609" alias="SC_EXP_47408_1#639" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282609</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#639</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B20, constructed from sample accession ERS13473040 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473040">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282579" alias="SC_EXP_47408_1#609" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282579</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#609</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L10, constructed from sample accession ERS13473010 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473010">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473010</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282318" alias="SC_EXP_47408_1#100" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282318</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O10, constructed from sample accession ERS13472778 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472778">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282651" alias="SC_EXP_47408_1#741" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282651</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#741</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:M6, constructed from sample accession ERS13472761 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472761">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472761</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:M6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282976" alias="SC_EXP_47423_1#235" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282976</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D23, constructed from sample accession ERS13472861 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472861">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472861</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282897" alias="SC_EXP_47423_1#156" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282897</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#156</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H1, constructed from sample accession ERS13472732 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472732">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472732</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283218" alias="SC_EXP_47423_1#779" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283218</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#779</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C16, constructed from sample accession ERS13472965 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282722" alias="SC_EXP_47408_1#907" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282722</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#907</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D2, constructed from sample accession ERS13473109 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282516" alias="SC_EXP_47408_1#452" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282516</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#452</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M16, constructed from sample accession ERS13472880 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472880">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282958" alias="SC_EXP_47423_1#217" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282958</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J17, constructed from sample accession ERS13472842 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282360" alias="SC_EXP_47408_1#142" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282360</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#142</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I22, constructed from sample accession ERS13472898 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472898">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283294" alias="SC_EXP_47423_1#855" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283294</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#855</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H11, constructed from sample accession ERS13472817 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472817">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282758" alias="SC_EXP_47408_1#943" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282758</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#943</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F12, constructed from sample accession ERS13473013 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473013">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473013</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282896" alias="SC_EXP_47423_1#155" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282896</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#155</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F1, constructed from sample accession ERS13472731 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472731">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282361" alias="SC_EXP_47408_1#143" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282361</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#143</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K22, constructed from sample accession ERS13472902 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282543" alias="SC_EXP_47408_1#479" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282543</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#479</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K24, constructed from sample accession ERS13472907 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472907">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472907</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282927" alias="SC_EXP_47423_1#186" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282927</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#186</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D9, constructed from sample accession ERS13472808 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472808">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282821" alias="SC_EXP_47423_1#80" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282821</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E6, constructed from sample accession ERS13472924 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472924">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472924</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282950" alias="SC_EXP_47423_1#209" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282950</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#209</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H15, constructed from sample accession ERS13472831 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282792" alias="SC_EXP_47408_1#977" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282792</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#977</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:F22, constructed from sample accession ERS13473048 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473048">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473048</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:F22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282631" alias="SC_EXP_47408_1#721" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282631</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#721</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:E2, constructed from sample accession ERS13472865 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472865">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472865</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283213" alias="SC_EXP_47423_1#774" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283213</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#774</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:I14, constructed from sample accession ERS13472961 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:I14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282477" alias="SC_EXP_47408_1#413" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282477</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#413</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O6, constructed from sample accession ERS13472760 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472760">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283460" alias="SC_EXP_47433_1#193" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283460</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#193</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F9, constructed from sample accession ERS13473164 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282889" alias="SC_EXP_47423_1#148" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282889</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G24, constructed from sample accession ERS13472994 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282877" alias="SC_EXP_47423_1#136" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282877</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#136</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K20, constructed from sample accession ERS13472982 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472982">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375994</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282594" alias="SC_EXP_47408_1#624" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282594</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#624</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N14, constructed from sample accession ERS13473026 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473026">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473026</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283037" alias="SC_EXP_47423_1#447" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283037</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#447</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:O14, constructed from sample accession ERS13472962 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282450" alias="SC_EXP_47408_1#326" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282450</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#326</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J24, constructed from sample accession ERS13473055 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282576" alias="SC_EXP_47408_1#606" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282576</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#606</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F10, constructed from sample accession ERS13473006 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282602" alias="SC_EXP_47408_1#632" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282602</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#632</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B18, constructed from sample accession ERS13473033 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282832" alias="SC_EXP_47423_1#91" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282832</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:K8, constructed from sample accession ERS13472936 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472936">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472936</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375949</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282828" alias="SC_EXP_47423_1#87" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282828</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C8, constructed from sample accession ERS13472931 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283443" alias="SC_EXP_47433_1#176" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283443</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#176</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H3, constructed from sample accession ERS13473147 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282796" alias="SC_EXP_47408_1#981" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282796</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#981</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B24, constructed from sample accession ERS13473052 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283394" alias="SC_EXP_47433_1#127" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283394</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#127</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K14, constructed from sample accession ERS13478586 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478586">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478586</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381606</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282951" alias="SC_EXP_47423_1#210" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282951</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#210</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J15, constructed from sample accession ERS13472832 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472832">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282553" alias="SC_EXP_47408_1#583" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282553</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#583</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:B4, constructed from sample accession ERS13473115 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282768" alias="SC_EXP_47408_1#953" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282768</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#953</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L14, constructed from sample accession ERS13473024 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282787" alias="SC_EXP_47408_1#972" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282787</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#972</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H20, constructed from sample accession ERS13473043 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282725" alias="SC_EXP_47408_1#910" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282725</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#910</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J2, constructed from sample accession ERS13473111 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473111">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473111</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282770" alias="SC_EXP_47408_1#955" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282770</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#955</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B16, constructed from sample accession ERS13473025 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473025">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282898" alias="SC_EXP_47423_1#157" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282898</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#157</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J1, constructed from sample accession ERS13472734 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472734">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472734</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283227" alias="SC_EXP_47423_1#788" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283227</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#788</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E18, constructed from sample accession ERS13472974 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282852" alias="SC_EXP_47423_1#111" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282852</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:C14, constructed from sample accession ERS13472956 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:C14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282389" alias="SC_EXP_47408_1#265" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282389</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#265</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:J6, constructed from sample accession ERS13473125 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282670" alias="SC_EXP_47408_1#760" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282670</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#760</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C12, constructed from sample accession ERS13472779 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472779">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472779</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282822" alias="SC_EXP_47423_1#81" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282822</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#81</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G6, constructed from sample accession ERS13472938 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282690" alias="SC_EXP_47408_1#780" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282690</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#780</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K16, constructed from sample accession ERS13472879 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472879">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282739" alias="SC_EXP_47408_1#924" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282739</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#924</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:J6, constructed from sample accession ERS13473125 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473125">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473125</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:J6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282956" alias="SC_EXP_47423_1#215" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282956</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:F17, constructed from sample accession ERS13472837 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472837">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472837</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282545" alias="SC_EXP_47408_1#481" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282545</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#481</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O24, constructed from sample accession ERS15395411 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400264</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282401" alias="SC_EXP_47408_1#277" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282401</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#277</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F10, constructed from sample accession ERS13473006 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376018</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282507" alias="SC_EXP_47408_1#443" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282507</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#443</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:K14, constructed from sample accession ERS13472791 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472791">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472791</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282964" alias="SC_EXP_47423_1#223" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282964</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#223</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:H19, constructed from sample accession ERS13472845 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:H19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282846" alias="SC_EXP_47423_1#105" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282846</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G12, constructed from sample accession ERS13472951 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282614" alias="SC_EXP_47408_1#644" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282614</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#644</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:L20, constructed from sample accession ERS13473045 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473045">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:L20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282865" alias="SC_EXP_47423_1#124" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282865</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#124</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M16, constructed from sample accession ERS13472970 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282743" alias="SC_EXP_47408_1#928" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282743</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#928</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:D8, constructed from sample accession ERS13473133 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473133">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282603" alias="SC_EXP_47408_1#633" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282603</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#633</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:D18, constructed from sample accession ERS13473034 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473034">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473034</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:D18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282789" alias="SC_EXP_47408_1#974" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282789</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#974</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L20, constructed from sample accession ERS13473045 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473045">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282288" alias="SC_EXP_47408_1#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282288</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:C4, constructed from sample accession ERS13472871 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472871">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282486" alias="SC_EXP_47408_1#422" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282486</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#422</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:A10, constructed from sample accession ERS13472771 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472771">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282926" alias="SC_EXP_47423_1#185" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282926</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#185</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B9, constructed from sample accession ERS13472807 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472807">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472807</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282766" alias="SC_EXP_47408_1#951" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282766</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#951</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:H14, constructed from sample accession ERS13473022 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473022">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473022</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:H14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282512" alias="SC_EXP_47408_1#448" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282512</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#448</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E16, constructed from sample accession ERS13472876 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472876">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282599" alias="SC_EXP_47408_1#629" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282599</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#629</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J16, constructed from sample accession ERS13473029 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282869" alias="SC_EXP_47423_1#128" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282869</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#128</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:E18, constructed from sample accession ERS13472974 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282826" alias="SC_EXP_47423_1#85" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282826</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:O6, constructed from sample accession ERS13472928 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:O6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282532" alias="SC_EXP_47408_1#468" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282532</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#468</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C22, constructed from sample accession ERS13472895 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282867" alias="SC_EXP_47423_1#126" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282867</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#126</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A18, constructed from sample accession ERS13472972 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472972">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282817" alias="SC_EXP_47423_1#76" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282817</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:M4, constructed from sample accession ERS13472923 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472923">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472923</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282279" alias="SC_EXP_47408_1#61" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282279</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A2, constructed from sample accession ERS13472863 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282443" alias="SC_EXP_47408_1#319" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282443</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H22, constructed from sample accession ERS13473049 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282899" alias="SC_EXP_47423_1#158" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282899</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#158</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L1, constructed from sample accession ERS13472735 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472735">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472735</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282784" alias="SC_EXP_47408_1#969" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282784</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#969</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:B20, constructed from sample accession ERS13473040 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473040">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473040</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:B20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282422" alias="SC_EXP_47408_1#298" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282422</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F16, constructed from sample accession ERS13473032 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282362" alias="SC_EXP_47408_1#144" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282362</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#144</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:M22, constructed from sample accession ERS13472904 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472904">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282835" alias="SC_EXP_47423_1#94" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282835</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#94</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A10, constructed from sample accession ERS13472941 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282910" alias="SC_EXP_47423_1#169" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282910</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#169</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B5, constructed from sample accession ERS13472744 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472744">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472744</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282711" alias="SC_EXP_47408_1#801" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282711</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#801</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:K22, constructed from sample accession ERS13472902 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282922" alias="SC_EXP_47423_1#181" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282922</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#181</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:J7, constructed from sample accession ERS13472802 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472802">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:J7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282380" alias="SC_EXP_47408_1#256" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282380</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#256</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F4, constructed from sample accession ERS13473119 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282559" alias="SC_EXP_47408_1#589" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282559</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#589</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N4, constructed from sample accession ERS13473120 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282908" alias="SC_EXP_47423_1#167" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282908</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#167</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:N3, constructed from sample accession ERS13472743 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472743">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472743</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:N3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282686" alias="SC_EXP_47408_1#776" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282686</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#776</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C16, constructed from sample accession ERS13472795 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472795">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472795</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282290" alias="SC_EXP_47408_1#72" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282290</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#72</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G4, constructed from sample accession ERS13472874 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472874">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282608" alias="SC_EXP_47408_1#638" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282608</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#638</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:N18, constructed from sample accession ERS13473039 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:N18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282501" alias="SC_EXP_47408_1#437" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282501</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#437</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:O12, constructed from sample accession ERS13472786 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472786">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472786</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:O12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282359" alias="SC_EXP_47408_1#141" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282359</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#141</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:G22, constructed from sample accession ERS13472899 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472899">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282871" alias="SC_EXP_47423_1#130" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282871</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#130</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:I18, constructed from sample accession ERS13472976 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472976">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472976</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:I18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282638" alias="SC_EXP_47408_1#728" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282638</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#728</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:C4, constructed from sample accession ERS13472871 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472871">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282334" alias="SC_EXP_47408_1#116" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282334</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#116</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:O14, constructed from sample accession ERS13472794 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472794">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472794</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282291" alias="SC_EXP_47408_1#73" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282291</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:I4, constructed from sample accession ERS13472875 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472875">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:I4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282332" alias="SC_EXP_47408_1#114" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282332</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K14, constructed from sample accession ERS13472791 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472791">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472791</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282335" alias="SC_EXP_47408_1#117" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282335</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#117</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:A16, constructed from sample accession ERS13472793 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472793">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472793</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:A16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282895" alias="SC_EXP_47423_1#154" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282895</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#154</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:D1, constructed from sample accession ERS13472733 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472733">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472733</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282544" alias="SC_EXP_47408_1#480" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282544</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#480</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:M24, constructed from sample accession ERS13472908 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GATTCATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:M24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282520" alias="SC_EXP_47408_1#456" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282520</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#456</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:E18, constructed from sample accession ERS13472884 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:E18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282539" alias="SC_EXP_47408_1#475" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282539</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#475</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:C24, constructed from sample accession ERS13472901 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472901">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282555" alias="SC_EXP_47408_1#585" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282555</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#585</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:F4, constructed from sample accession ERS13473119 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282747" alias="SC_EXP_47408_1#932" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282747</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#932</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20806-R:L8, constructed from sample accession ERS13473134 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20806-R:L8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282854" alias="SC_EXP_47423_1#113" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282854</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:G14, constructed from sample accession ERS13472958 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282968" alias="SC_EXP_47423_1#227" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282968</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#227</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:B21, constructed from sample accession ERS13472849 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472849">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472849</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:B21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282619" alias="SC_EXP_47408_1#649" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282619</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#649</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20757-C:J22, constructed from sample accession ERS13473050 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473050">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20757-C:J22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282373" alias="SC_EXP_47408_1#249" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282373</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#249</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:F2, constructed from sample accession ERS13473108 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282433" alias="SC_EXP_47408_1#309" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282433</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:N18, constructed from sample accession ERS13473039 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GTGTCCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:N18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282329" alias="SC_EXP_47408_1#111" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282329</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:E14, constructed from sample accession ERS13472792 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472792">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472792</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:E14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282811" alias="SC_EXP_47423_1#70" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282811</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#70</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:A4, constructed from sample accession ERS13472916 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472916">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282409" alias="SC_EXP_47408_1#285" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282409</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#285</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:H12, constructed from sample accession ERS13473014 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376026</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282420" alias="SC_EXP_47408_1#296" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282420</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:B16, constructed from sample accession ERS13473025 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473025">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473025</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:B16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282439" alias="SC_EXP_47408_1#315" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282439</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:L20, constructed from sample accession ERS13473045 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473045">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473045</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:L20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282368" alias="SC_EXP_47408_1#150" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282368</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47408_1#150</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20639-U:K24, constructed from sample accession ERS13472907 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47408_1).  This submission includes reads tagged with the sequence GCTAACTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472907">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472907</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20639-U:K24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282966" alias="SC_EXP_47423_1#225" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282966</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#225</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20640-N:L19, constructed from sample accession ERS13472847 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472847">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472847</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20640-N:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283055" alias="SC_EXP_47423_1#465" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283055</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#465</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:I20, constructed from sample accession ERS13472981 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GAGGTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472981">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472981</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:I20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283370" alias="SC_EXP_47433_1#103" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283370</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:K8, constructed from sample accession ERS13478562 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478562">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478562</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381585</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:K8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283396" alias="SC_EXP_47433_1#129" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283396</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#129</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:O14, constructed from sample accession ERS13478588 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478588">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478588</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283268" alias="SC_EXP_47423_1#829" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283268</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#829</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:B5, constructed from sample accession ERS13472744 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472744">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472744</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283157" alias="SC_EXP_47423_1#567" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283157</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#567</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H23, constructed from sample accession ERS13472858 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472858">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472858</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283310" alias="SC_EXP_47423_1#871" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283310</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#871</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L15, constructed from sample accession ERS13472833 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472833">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472833</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283061" alias="SC_EXP_47423_1#471" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283061</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#471</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G22, constructed from sample accession ERS13472986 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283324" alias="SC_EXP_47423_1#885" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283324</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#885</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L19, constructed from sample accession ERS13472847 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCATGGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472847">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472847</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283245" alias="SC_EXP_47423_1#806" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283245</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#806</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:C24, constructed from sample accession ERS13472991 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:C24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283090" alias="SC_EXP_47423_1#500" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283090</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#500</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D5, constructed from sample accession ERS13472755 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472755">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472755</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375768</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283064" alias="SC_EXP_47423_1#474" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283064</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#474</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M22, constructed from sample accession ERS13472990 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGATTAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472990">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283216" alias="SC_EXP_47423_1#777" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283216</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#777</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:O14, constructed from sample accession ERS13472962 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:O14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283123" alias="SC_EXP_47423_1#533" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283123</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#533</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J13, constructed from sample accession ERS13472824 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472824">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472824</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283467" alias="SC_EXP_47433_1#200" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283467</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#200</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H11, constructed from sample accession ERS13473171 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473171">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473171</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283091" alias="SC_EXP_47423_1#501" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283091</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#501</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F5, constructed from sample accession ERS13472749 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472749">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472749</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283017" alias="SC_EXP_47423_1#427" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283017</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#427</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:G10, constructed from sample accession ERS13472942 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283502" alias="SC_EXP_47433_1#235" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283502</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#235</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H23, constructed from sample accession ERS13473207 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCCTGTTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473207">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473207</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283337" alias="SC_EXP_47423_1#899" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283337</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#899</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J23, constructed from sample accession ERS13472860 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCACTGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283196" alias="SC_EXP_47423_1#757" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283196</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#757</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G10, constructed from sample accession ERS13472942 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283366" alias="SC_EXP_47433_1#99" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283366</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#99</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C8, constructed from sample accession ERS13478558 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478558">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478558</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381578</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283063" alias="SC_EXP_47423_1#473" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283063</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#473</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:K22, constructed from sample accession ERS13472988 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTTGTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:K22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283040" alias="SC_EXP_47423_1#450" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283040</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#450</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E16, constructed from sample accession ERS13472969 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283188" alias="SC_EXP_47423_1#749" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283188</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#749</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G8, constructed from sample accession ERS13472932 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472932">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472932</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283254" alias="SC_EXP_47423_1#815" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283254</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#815</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F1, constructed from sample accession ERS13472731 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472731">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283006" alias="SC_EXP_47423_1#416" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283006</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#416</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A8, constructed from sample accession ERS13472929 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472929">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472929</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283293" alias="SC_EXP_47423_1#854" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283293</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#854</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F11, constructed from sample accession ERS13472816 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472816">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283028" alias="SC_EXP_47423_1#438" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283028</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#438</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M12, constructed from sample accession ERS13472954 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283212" alias="SC_EXP_47423_1#773" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283212</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#773</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:G14, constructed from sample accession ERS13472958 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:G14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283237" alias="SC_EXP_47423_1#798" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283237</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#798</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A22, constructed from sample accession ERS13472983 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375995</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283106" alias="SC_EXP_47423_1#516" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283106</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#516</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D9, constructed from sample accession ERS13472808 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472808">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283096" alias="SC_EXP_47423_1#506" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283096</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#506</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:P5, constructed from sample accession ERS13472797 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472797">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:P5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283132" alias="SC_EXP_47423_1#542" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283132</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#542</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N15, constructed from sample accession ERS13472834 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472834">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283329" alias="SC_EXP_47423_1#891" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283329</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#891</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H21, constructed from sample accession ERS13472852 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTAAGGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472852">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472852</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283426" alias="SC_EXP_47433_1#159" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283426</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#159</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A24, constructed from sample accession ERS13478618 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478618">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478618</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381638</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283113" alias="SC_EXP_47423_1#523" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283113</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#523</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:D11, constructed from sample accession ERS13472815 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472815">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472815</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283287" alias="SC_EXP_47423_1#848" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283287</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#848</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:H9, constructed from sample accession ERS13472810 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472810">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472810</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283052" alias="SC_EXP_47423_1#462" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283052</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#462</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:A20, constructed from sample accession ERS13472978 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472978">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472978</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:A20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283484" alias="SC_EXP_47433_1#217" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283484</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#217</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F17, constructed from sample accession ERS13473188 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473188">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376200</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283303" alias="SC_EXP_47423_1#864" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283303</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#864</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L13, constructed from sample accession ERS13472826 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472826">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283239" alias="SC_EXP_47423_1#800" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283239</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#800</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E22, constructed from sample accession ERS13472984 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GCTCCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283100" alias="SC_EXP_47423_1#510" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283100</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#510</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:H7, constructed from sample accession ERS13472801 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472801">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283463" alias="SC_EXP_47433_1#196" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283463</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#196</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L9, constructed from sample accession ERS13473165 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473165">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473165</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283119" alias="SC_EXP_47423_1#529" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283119</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#529</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:B13, constructed from sample accession ERS13472825 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472825">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:B13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283171" alias="SC_EXP_47423_1#732" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283171</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#732</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:E4, constructed from sample accession ERS13472917 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283419" alias="SC_EXP_47433_1#152" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283419</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#152</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:A22, constructed from sample accession ERS13478611 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GGAATGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478611">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478611</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381631</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:A22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283099" alias="SC_EXP_47423_1#509" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283099</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#509</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:F7, constructed from sample accession ERS13472800 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472800">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472800</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283439" alias="SC_EXP_47433_1#172" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283439</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#172</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:L1, constructed from sample accession ERS13473145 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473145">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:L1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283281" alias="SC_EXP_47423_1#842" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283281</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#842</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:L7, constructed from sample accession ERS13472804 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472804">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:L7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283288" alias="SC_EXP_47423_1#849" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283288</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#849</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:J9, constructed from sample accession ERS13472811 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472811">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283344" alias="SC_EXP_47433_1#77" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283344</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G2, constructed from sample accession ERS13478536 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478536">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478536</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381556</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283406" alias="SC_EXP_47433_1#139" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283406</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#139</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:C18, constructed from sample accession ERS13478597 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478597">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478597</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381618</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:C18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283244" alias="SC_EXP_47423_1#805" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283244</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#805</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:A24, constructed from sample accession ERS13472992 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTGTGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472992">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472992</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:A24</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283103" alias="SC_EXP_47423_1#513" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283103</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#513</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:N7, constructed from sample accession ERS13472806 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472806">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472806</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:N7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283109" alias="SC_EXP_47423_1#519" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283109</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#519</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:J9, constructed from sample accession ERS13472811 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472811">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:J9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283488" alias="SC_EXP_47433_1#221" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283488</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#221</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B19, constructed from sample accession ERS13473191 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GCAACATT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473191">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283415" alias="SC_EXP_47433_1#148" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283415</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#148</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:G20, constructed from sample accession ERS13478607 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GTACATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478607">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478607</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381630</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:G20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283466" alias="SC_EXP_47433_1#199" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283466</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#199</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:F11, constructed from sample accession ERS13473169 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473169">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473169</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283000" alias="SC_EXP_47423_1#410" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283000</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#410</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:E6, constructed from sample accession ERS13472924 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472924">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472924</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11282996" alias="SC_EXP_47423_1#406" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11282996</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#406</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:M4, constructed from sample accession ERS13472923 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472923">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472923</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:M4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283440" alias="SC_EXP_47433_1#173" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283440</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#173</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B3, constructed from sample accession ERS13473144 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473144">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283267" alias="SC_EXP_47423_1#828" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283267</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#828</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:P3, constructed from sample accession ERS13472746 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472746">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472746</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:P3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283262" alias="SC_EXP_47423_1#823" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283262</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#823</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:F3, constructed from sample accession ERS13472740 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13472740">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13472740</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111375752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283449" alias="SC_EXP_47433_1#182" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283449</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#182</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:H5, constructed from sample accession ERS13473153 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473153">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283340" alias="SC_EXP_47423_1#902" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283340</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#902</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20807-S:P23, constructed from sample accession ERS15395410 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20807-S:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283401" alias="SC_EXP_47433_1#134" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283401</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#134</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:I16, constructed from sample accession ERS13478593 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13478593">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13478593</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111381613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:I16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283482" alias="SC_EXP_47433_1#215" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283482</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47433_1#215</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20633-O:B17, constructed from sample accession ERS13473185 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47433_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS13473185">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS13473185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA111376197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20633-O:B17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11283161" alias="SC_EXP_47423_1#571" center_name="Wellcome Sanger Institute">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11283161</PRIMARY_ID>
      <SUBMITTER_ID namespace="Wellcome Sanger Institute">SC_EXP_47423_1#571</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina MiSeq 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 SQPP-20758-D:P23, constructed from sample accession ERS15395410 for study accession ERP000190.  This is part of an Illumina multiplexed sequencing run (47423_1).  This submission includes reads tagged with the sequence GTCTTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS15395410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS15395410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA113400263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>SQPP-20758-D:P23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>GBS</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
