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    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:B1, constructed from sample accession ERS1903623 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903623">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903623</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278645</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#9" accession="ERX2663080">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C2, constructed from sample accession ERS1903632 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903632">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903632</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278654</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="365" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#12" accession="ERX2663081">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:G2, constructed from sample accession ERS1903636 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903636">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903636</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278658</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#15" accession="ERX2663082">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:B3, constructed from sample accession ERS1903639 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903639">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903639</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278661</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="353" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#18" accession="ERX2663083">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:E3, constructed from sample accession ERS1903642 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903642">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903642</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278664</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#21" accession="ERX2663084">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:H3, constructed from sample accession ERS1903645 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903645">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903645</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278667</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#24" accession="ERX2663085">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C4, constructed from sample accession ERS1903648 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903648">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903648</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278670</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#27" accession="ERX2663086">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:G4, constructed from sample accession ERS1903652 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903652">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903652</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278674</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_6#30" accession="ERX2663087">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_6#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_6#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:B5, constructed from sample accession ERS1903655 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_6).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903655">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903655</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278677</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#2" accession="ERX2663088">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C1, constructed from sample accession ERS1903624 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903624">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903624</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278646</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#10" accession="ERX2663089">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D2, constructed from sample accession ERS1903633 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903633">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903633</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278655</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#13" accession="ERX2663090">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:H2, constructed from sample accession ERS1903637 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903637">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903637</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278659</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="345" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#16" accession="ERX2663091">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C3, constructed from sample accession ERS1903640 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903640">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903640</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278662</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="353" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#19" accession="ERX2663092">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:F3, constructed from sample accession ERS1903643 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903643">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903643</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278665</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#22" accession="ERX2663093">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:A4, constructed from sample accession ERS1903646 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903646">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903646</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278668</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="342" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#25" accession="ERX2663094">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D4, constructed from sample accession ERS1903649 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903649">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903649</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278671</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#28" accession="ERX2663095">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:H4, constructed from sample accession ERS1903653 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903653">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903653</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278675</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_7#31" accession="ERX2663096">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_7#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_7#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C5, constructed from sample accession ERS1903656 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903656">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903656</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278678</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#3" accession="ERX2663097">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D1, constructed from sample accession ERS1903625 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903625">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903625</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278647</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="346" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#11" accession="ERX2663098">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:E2, constructed from sample accession ERS1903634 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903634">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903634</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278656</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#14" accession="ERX2663099">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:A3, constructed from sample accession ERS1903638 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903638">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903638</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278660</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="332" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#17" accession="ERX2663100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D3, constructed from sample accession ERS1903641 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903641">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903641</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278663</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#20" accession="ERX2663101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:G3, constructed from sample accession ERS1903644 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903644">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903644</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278666</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#23" accession="ERX2663102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:B4, constructed from sample accession ERS1903647 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903647">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903647</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278669</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#26" accession="ERX2663103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:F4, constructed from sample accession ERS1903651 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903651">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903651</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278673</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="373" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24073_8#29" accession="ERX2663104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24073_8#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24073_8#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:A5, constructed from sample accession ERS1903654 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24073_8).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903654">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903654</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278676</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_1#1" accession="ERX2663105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A10, constructed from sample accession ERS1888400 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_1).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888400">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_1#4" accession="ERX2663106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B10, constructed from sample accession ERS1888401 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_1).  This submission includes reads tagged with the sequence ACGTATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888401">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="167"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_1#12" accession="ERX2663107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D12, constructed from sample accession ERS1888419 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_1).  This submission includes reads tagged with the sequence GAGCTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_1#15" accession="ERX2663108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E12, constructed from sample accession ERS1888420 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_1).  This submission includes reads tagged with the sequence TAGGATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888420">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_1#18" accession="ERX2663109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F12, constructed from sample accession ERS1888422 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_1).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888422">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229404</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_1#21" accession="ERX2663110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G12, constructed from sample accession ERS1888423 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_1).  This submission includes reads tagged with the sequence CACCTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888423">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229405</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="3"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_1#24" accession="ERX2663111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H12, constructed from sample accession ERS1888424 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_1).  This submission includes reads tagged with the sequence GCCAAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888424">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229406</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="186"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_2#3" accession="ERX2663112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A12, constructed from sample accession ERS1888416 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_2).  This submission includes reads tagged with the sequence AGTACAAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888416">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229398</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="521" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_2#6" accession="ERX2663113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B12, constructed from sample accession ERS1888417 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_2).  This submission includes reads tagged with the sequence AGAGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888417">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:B12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="277" NOMINAL_SDEV="196"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_2#9" accession="ERX2663114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C12, constructed from sample accession ERS1888418 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_2).  This submission includes reads tagged with the sequence CCAGTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888418">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229400</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="319" NOMINAL_SDEV="181"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_2#12" accession="ERX2663115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D12, constructed from sample accession ERS1888419 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_2).  This submission includes reads tagged with the sequence GAGCTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888419">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229401</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_2#20" accession="ERX2663116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G11, constructed from sample accession ERS1888414 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_2).  This submission includes reads tagged with the sequence CAAGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_2#23" accession="ERX2663117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H11, constructed from sample accession ERS1888415 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_2).  This submission includes reads tagged with the sequence GATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888415">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229397</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="381" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_3#2" accession="ERX2663118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A11, constructed from sample accession ERS1888408 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_3).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888408">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_3#5" accession="ERX2663119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B11, constructed from sample accession ERS1888409 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_3).  This submission includes reads tagged with the sequence ACTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888409">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229391</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="469" NOMINAL_SDEV="328"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_3#8" accession="ERX2663120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C11, constructed from sample accession ERS1888410 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_3).  This submission includes reads tagged with the sequence CATACCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888410">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229392</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="484" NOMINAL_SDEV="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_3#11" accession="ERX2663121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D11, constructed from sample accession ERS1888411 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_3).  This submission includes reads tagged with the sequence CAAGACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888411">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="293" NOMINAL_SDEV="242"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_3#14" accession="ERX2663122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E11, constructed from sample accession ERS1888412 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_3).  This submission includes reads tagged with the sequence GTGTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888412">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="515" NOMINAL_SDEV="205"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_3#17" accession="ERX2663123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F11, constructed from sample accession ERS1888413 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_3).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888413">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229395</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="248" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24114_3#20" accession="ERX2663124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24114_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24114_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G11, constructed from sample accession ERS1888414 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24114_3).  This submission includes reads tagged with the sequence CAAGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888414">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="115"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24151_1#4" accession="ERX2663125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24151_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24151_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B7, constructed from sample accession ERS1888357 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24151_1).  This submission includes reads tagged with the sequence ACAGCAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24151_1#7" accession="ERX2663126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24151_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24151_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C7, constructed from sample accession ERS1888359 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24151_1).  This submission includes reads tagged with the sequence GACTAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888359">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229341</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="160"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24151_1#10" accession="ERX2663127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24151_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24151_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D7, constructed from sample accession ERS1888362 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24151_1).  This submission includes reads tagged with the sequence CTCAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888362">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24151_1#13" accession="ERX2663128">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663128</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24151_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24151_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E7, constructed from sample accession ERS1888366 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24151_1).  This submission includes reads tagged with the sequence GGTGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229348</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="328" NOMINAL_SDEV="162"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24151_1#16" accession="ERX2663129">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663129</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24151_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24151_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F7, constructed from sample accession ERS1888369 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24151_1).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888369">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229351</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24151_1#19" accession="ERX2663130">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663130</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24151_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24151_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G7, constructed from sample accession ERS1888371 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24151_1).  This submission includes reads tagged with the sequence AGGCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="198"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24151_1#22" accession="ERX2663131">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663131</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24151_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24151_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H7, constructed from sample accession ERS1888373 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24151_1).  This submission includes reads tagged with the sequence CTAAGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888373">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_1#1" accession="ERX2663132">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663132</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A7, constructed from sample accession ERS1888356 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229338</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_1#4" accession="ERX2663133">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663133</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B7, constructed from sample accession ERS1888357 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_1).  This submission includes reads tagged with the sequence ACAGCAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229339</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_1#12" accession="ERX2663134">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663134</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D9, constructed from sample accession ERS1888395 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_1).  This submission includes reads tagged with the sequence CTGGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888395">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="217" NOMINAL_SDEV="2"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_1#15" accession="ERX2663135">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663135</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E9, constructed from sample accession ERS1888396 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_1).  This submission includes reads tagged with the sequence GTCGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888396">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="271"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_1#18" accession="ERX2663136">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663136</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F9, constructed from sample accession ERS1888397 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_1).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888397">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="194" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_1#21" accession="ERX2663137">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663137</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G9, constructed from sample accession ERS1888398 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_1).  This submission includes reads tagged with the sequence ATCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888398">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_1#24" accession="ERX2663138">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663138</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H9, constructed from sample accession ERS1888399 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_1).  This submission includes reads tagged with the sequence GACAGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888399">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229381</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_2#3" accession="ERX2663139">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663139</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A9, constructed from sample accession ERS1888388 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_2).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888388">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_2#6" accession="ERX2663140">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663140</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B9, constructed from sample accession ERS1888389 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_2).  This submission includes reads tagged with the sequence ACGCTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888389">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_2#9" accession="ERX2663141">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663141</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C9, constructed from sample accession ERS1888391 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_2).  This submission includes reads tagged with the sequence CACTTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888391">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="339"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_2#20" accession="ERX2663142">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663142</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G8, constructed from sample accession ERS1888385 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_2).  This submission includes reads tagged with the sequence ATAGCGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888385">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229367</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_2#23" accession="ERX2663143">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663143</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H8, constructed from sample accession ERS1888386 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_2).  This submission includes reads tagged with the sequence GAACAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888386">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_3#2" accession="ERX2663144">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663144</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:A2, constructed from sample accession ERS1888446 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_3).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888446">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_3#5" accession="ERX2663145">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663145</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:B2, constructed from sample accession ERS1888447 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_3).  This submission includes reads tagged with the sequence AACCGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888447">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="224" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_3#8" accession="ERX2663146">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663146</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:C2, constructed from sample accession ERS1888448 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_3).  This submission includes reads tagged with the sequence AGCAGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888448">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="318" NOMINAL_SDEV="164"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_3#11" accession="ERX2663147">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663147</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:D2, constructed from sample accession ERS1888449 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_3).  This submission includes reads tagged with the sequence CCGTGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888449">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="201" NOMINAL_SDEV="43"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_3#14" accession="ERX2663148">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663148</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:E2, constructed from sample accession ERS1888451 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_3).  This submission includes reads tagged with the sequence GCCACATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888451">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="204" NOMINAL_SDEV="70"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_3#17" accession="ERX2663149">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663149</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:F2, constructed from sample accession ERS1888452 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_3).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888452">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="181" NOMINAL_SDEV="18"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_4#4" accession="ERX2663150">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663150</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:B1, constructed from sample accession ERS1888428 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_4).  This submission includes reads tagged with the sequence AACAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888428">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229410</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_4#7" accession="ERX2663151">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663151</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:C1, constructed from sample accession ERS1888429 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_4).  This submission includes reads tagged with the sequence AGATCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888429">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229411</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="208" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_4#10" accession="ERX2663152">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663152</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:D1, constructed from sample accession ERS1888430 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_4).  This submission includes reads tagged with the sequence CCGAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888430">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229412</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="227" NOMINAL_SDEV="156"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_4#13" accession="ERX2663153">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663153</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:E1, constructed from sample accession ERS1888438 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_4).  This submission includes reads tagged with the sequence GATAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888438">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_4#16" accession="ERX2663154">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663154</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:F1, constructed from sample accession ERS1888439 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_4).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888439">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229421</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="185" NOMINAL_SDEV="204"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_4#19" accession="ERX2663155">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663155</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:G1, constructed from sample accession ERS1888440 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_4).  This submission includes reads tagged with the sequence AATGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888440">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="190" NOMINAL_SDEV="19"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_4#22" accession="ERX2663156">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663156</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:H1, constructed from sample accession ERS1888442 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_4).  This submission includes reads tagged with the sequence CCATCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888442">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_5#1" accession="ERX2663157">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663157</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:A1, constructed from sample accession ERS1888426 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_5).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888426">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229408</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="161" NOMINAL_SDEV="11"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_5#12" accession="ERX2663158">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663158</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:D3, constructed from sample accession ERS1888463 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_5).  This submission includes reads tagged with the sequence CCTCCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888463">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229445</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="214" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_5#15" accession="ERX2663159">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:E3, constructed from sample accession ERS1888465 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_5).  This submission includes reads tagged with the sequence GCGAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888465">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229447</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_5#18" accession="ERX2663160">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:F3, constructed from sample accession ERS1888466 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_5).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888466">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888466</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229448</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="188" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_5#21" accession="ERX2663161">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:G3, constructed from sample accession ERS1888467 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_5).  This submission includes reads tagged with the sequence ACAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888467">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888467</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229449</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="175" NOMINAL_SDEV="20"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_5#24" accession="ERX2663162">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663162</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:H3, constructed from sample accession ERS1888468 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_5).  This submission includes reads tagged with the sequence CCTAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888468">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888468</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229450</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="203" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_6#3" accession="ERX2663163">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663163</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:A6, constructed from sample accession ERS1888492 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_6).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888492">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888492</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_6#6" accession="ERX2663164">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663164</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:B6, constructed from sample accession ERS1888493 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_6).  This submission includes reads tagged with the sequence ACACAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888493">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="196"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_6#9" accession="ERX2663165">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663165</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:C6, constructed from sample accession ERS1888494 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_6).  This submission includes reads tagged with the sequence CAACCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888494">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888494</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="212" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_6#20" accession="ERX2663166">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663166</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:G6, constructed from sample accession ERS1888499 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_6).  This submission includes reads tagged with the sequence AGCCATGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888499">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888499</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="264" NOMINAL_SDEV="144"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_6#23" accession="ERX2663167">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663167</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:H6, constructed from sample accession ERS1888500 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_6).  This submission includes reads tagged with the sequence CGGATTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888500">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888500</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_7#3" accession="ERX2663168">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663168</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:A6, constructed from sample accession ERS1888492 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_7).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888492">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888492</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="458"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_7#6" accession="ERX2663169">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663169</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:B6, constructed from sample accession ERS1888493 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_7).  This submission includes reads tagged with the sequence ACACAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888493">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="182"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_7#9" accession="ERX2663170">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663170</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:C6, constructed from sample accession ERS1888494 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_7).  This submission includes reads tagged with the sequence CAACCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888494">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888494</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="207" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_7#12" accession="ERX2663171">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663171</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:D6, constructed from sample accession ERS1888496 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_7).  This submission includes reads tagged with the sequence CGCATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888496">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888496</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="50"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_7#15" accession="ERX2663172">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663172</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:E6, constructed from sample accession ERS1888497 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_7).  This submission includes reads tagged with the sequence GGAGAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888497">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888497</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_7#18" accession="ERX2663173">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663173</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:G4, constructed from sample accession ERS1888478 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_7).  This submission includes reads tagged with the sequence AGATGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="196" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_8#6" accession="ERX2663174">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663174</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:B6, constructed from sample accession ERS1888493 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_8).  This submission includes reads tagged with the sequence ACACAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888493">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888493</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320" NOMINAL_SDEV="188"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_8#9" accession="ERX2663175">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663175</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:C6, constructed from sample accession ERS1888494 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_8).  This submission includes reads tagged with the sequence CAACCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888494">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888494</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="207" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_8#12" accession="ERX2663176">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663176</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:D6, constructed from sample accession ERS1888496 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_8).  This submission includes reads tagged with the sequence CGCATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888496">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888496</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="194"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_8#15" accession="ERX2663177">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663177</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_8#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:E6, constructed from sample accession ERS1888497 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_8).  This submission includes reads tagged with the sequence GGAGAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888497">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888497</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="462" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_8#18" accession="ERX2663178">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663178</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:G4, constructed from sample accession ERS1888478 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_8).  This submission includes reads tagged with the sequence AGATGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="47"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24177_8#21" accession="ERX2663179">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663179</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24177_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24177_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495720E:H4, constructed from sample accession ERS1888480 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24177_8).  This submission includes reads tagged with the sequence CCTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888480">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888480</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495720E:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="208" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#1" accession="ERX2663180">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663180</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D5, constructed from sample accession ERS1904000 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#4" accession="ERX2663181">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663181</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:G5, constructed from sample accession ERS1904003 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904003">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#7" accession="ERX2663182">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663182</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:B6, constructed from sample accession ERS1904006 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279028</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#15" accession="ERX2663183">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663183</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:B7, constructed from sample accession ERS1904014 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#18" accession="ERX2663184">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663184</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:E7, constructed from sample accession ERS1904024 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#21" accession="ERX2663185">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663185</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:H7, constructed from sample accession ERS1904027 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#24" accession="ERX2663186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C8, constructed from sample accession ERS1904030 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#27" accession="ERX2663187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:F8, constructed from sample accession ERS1904033 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#30" accession="ERX2663188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:A9, constructed from sample accession ERS1904036 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_1#33" accession="ERX2663189">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663189</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D9, constructed from sample accession ERS1904039 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#1" accession="ERX2663190">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663190</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D5, constructed from sample accession ERS1904000 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#4" accession="ERX2663191">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663191</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:G5, constructed from sample accession ERS1904003 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904003">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279025</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#12" accession="ERX2663192">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663192</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:G6, constructed from sample accession ERS1904011 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#15" accession="ERX2663193">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663193</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:B7, constructed from sample accession ERS1904014 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#18" accession="ERX2663194">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663194</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:E7, constructed from sample accession ERS1904024 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#21" accession="ERX2663195">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663195</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:H7, constructed from sample accession ERS1904027 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#24" accession="ERX2663196">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663196</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C8, constructed from sample accession ERS1904030 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#27" accession="ERX2663197">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663197</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:F8, constructed from sample accession ERS1904033 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#30" accession="ERX2663198">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663198</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:A9, constructed from sample accession ERS1904036 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_2#33" accession="ERX2663199">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663199</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D9, constructed from sample accession ERS1904039 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_2).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#1" accession="ERX2663200">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663200</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D5, constructed from sample accession ERS1904000 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904000">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904000</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279022</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#9" accession="ERX2663201">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663201</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D6, constructed from sample accession ERS1904008 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279030</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#12" accession="ERX2663202">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663202</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:G6, constructed from sample accession ERS1904011 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904011">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904011</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279033</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#15" accession="ERX2663203">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663203</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:B7, constructed from sample accession ERS1904014 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#18" accession="ERX2663204">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663204</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:E7, constructed from sample accession ERS1904024 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904024">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904024</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#21" accession="ERX2663205">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663205</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:H7, constructed from sample accession ERS1904027 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#24" accession="ERX2663206">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663206</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C8, constructed from sample accession ERS1904030 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904030">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904030</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#27" accession="ERX2663207">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663207</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:F8, constructed from sample accession ERS1904033 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904033">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904033</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#30" accession="ERX2663208">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663208</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:A9, constructed from sample accession ERS1904036 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904036">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904036</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_3#33" accession="ERX2663209">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663209</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D9, constructed from sample accession ERS1904039 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_3).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904039">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904039</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#6" accession="ERX2663210">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663210</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H1, constructed from sample accession ERS1904263 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#9" accession="ERX2663211">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663211</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:D2, constructed from sample accession ERS1904251 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#12" accession="ERX2663212">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663212</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:G2, constructed from sample accession ERS1904254 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#15" accession="ERX2663213">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663213</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:B3, constructed from sample accession ERS1904269 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#18" accession="ERX2663214">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663214</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:E3, constructed from sample accession ERS1904272 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#21" accession="ERX2663215">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663215</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H3, constructed from sample accession ERS1904275 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#24" accession="ERX2663216">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663216</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:C4, constructed from sample accession ERS1904278 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#27" accession="ERX2663217">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663217</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F4, constructed from sample accession ERS1904281 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_4#30" accession="ERX2663218">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663218</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_4#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_4#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:A5, constructed from sample accession ERS1904284 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_4).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#6" accession="ERX2663219">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663219</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H1, constructed from sample accession ERS1904263 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="373" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#9" accession="ERX2663220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:D2, constructed from sample accession ERS1904251 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#12" accession="ERX2663221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:G2, constructed from sample accession ERS1904254 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#15" accession="ERX2663222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:B3, constructed from sample accession ERS1904269 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#18" accession="ERX2663223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:E3, constructed from sample accession ERS1904272 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#21" accession="ERX2663224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H3, constructed from sample accession ERS1904275 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#24" accession="ERX2663225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:C4, constructed from sample accession ERS1904278 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#27" accession="ERX2663226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F4, constructed from sample accession ERS1904281 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_5#30" accession="ERX2663227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_5#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:A5, constructed from sample accession ERS1904284 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_5).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#6" accession="ERX2663228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H1, constructed from sample accession ERS1904263 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279285</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#9" accession="ERX2663229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:D2, constructed from sample accession ERS1904251 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279273</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#12" accession="ERX2663230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:G2, constructed from sample accession ERS1904254 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904254">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#15" accession="ERX2663231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:B3, constructed from sample accession ERS1904269 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279291</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#18" accession="ERX2663232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:E3, constructed from sample accession ERS1904272 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904272">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#21" accession="ERX2663233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H3, constructed from sample accession ERS1904275 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904275">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#24" accession="ERX2663234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:C4, constructed from sample accession ERS1904278 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#27" accession="ERX2663235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F4, constructed from sample accession ERS1904281 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_6#30" accession="ERX2663236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_6#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_6#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:A5, constructed from sample accession ERS1904284 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_6).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904284">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#6" accession="ERX2663237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:A6, constructed from sample accession ERS1904292 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#9" accession="ERX2663238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:D6, constructed from sample accession ERS1904295 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#12" accession="ERX2663239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:G6, constructed from sample accession ERS1904298 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="455" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#15" accession="ERX2663240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:B7, constructed from sample accession ERS1904301 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#18" accession="ERX2663241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:E7, constructed from sample accession ERS1904304 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#21" accession="ERX2663242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H7, constructed from sample accession ERS1904307 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#24" accession="ERX2663243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:C8, constructed from sample accession ERS1904310 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_7#27" accession="ERX2663244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_7#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_7#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F8, constructed from sample accession ERS1904313 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904313">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279335</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#3" accession="ERX2663245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F5, constructed from sample accession ERS1904289 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#6" accession="ERX2663246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:A6, constructed from sample accession ERS1904292 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#9" accession="ERX2663247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:D6, constructed from sample accession ERS1904295 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#12" accession="ERX2663248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:G6, constructed from sample accession ERS1904298 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#15" accession="ERX2663249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:B7, constructed from sample accession ERS1904301 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#18" accession="ERX2663250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:E7, constructed from sample accession ERS1904304 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#21" accession="ERX2663251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H7, constructed from sample accession ERS1904307 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#24" accession="ERX2663252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:C8, constructed from sample accession ERS1904310 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24178_8#35" accession="ERX2663253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24178_8#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24178_8#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F9, constructed from sample accession ERS1904321 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24178_8).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_7#3" accession="ERX2663254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A3, constructed from sample accession ERS1887960 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_7).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322" NOMINAL_SDEV="178"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_7#6" accession="ERX2663255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B3, constructed from sample accession ERS1887962 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_7).  This submission includes reads tagged with the sequence AACGCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="463" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_7#9" accession="ERX2663256">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C3, constructed from sample accession ERS1887964 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_7).  This submission includes reads tagged with the sequence AGTCACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228946</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_7#12" accession="ERX2663257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D3, constructed from sample accession ERS1887965 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_7).  This submission includes reads tagged with the sequence CCTCCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="319" NOMINAL_SDEV="136"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_7#15" accession="ERX2663258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E3, constructed from sample accession ERS1887966 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_7).  This submission includes reads tagged with the sequence GCGAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228948</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="473" NOMINAL_SDEV="161"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_7#18" accession="ERX2663259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F3, constructed from sample accession ERS1887970 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_7).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887970">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887970</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228952</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="454" NOMINAL_SDEV="173"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_7#21" accession="ERX2663260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G3, constructed from sample accession ERS1887972 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_7).  This submission includes reads tagged with the sequence ACAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887972">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887972</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228954</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="273" NOMINAL_SDEV="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_8#8" accession="ERX2663261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C5, constructed from sample accession ERS1887984 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_8).  This submission includes reads tagged with the sequence ATTGAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="510" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_8#11" accession="ERX2663262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D5, constructed from sample accession ERS1887985 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_8).  This submission includes reads tagged with the sequence CGACTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="223"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_8#14" accession="ERX2663263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_8#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E5, constructed from sample accession ERS1887986 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_8).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="478" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_8#17" accession="ERX2663264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_8#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F5, constructed from sample accession ERS1887987 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_8).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="188" NOMINAL_SDEV="23"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_8#20" accession="ERX2663265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_8#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G5, constructed from sample accession ERS1887988 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_8).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="240"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24185_8#23" accession="ERX2663266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24185_8#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24185_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H5, constructed from sample accession ERS1887989 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24185_8).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#2" accession="ERX2663267">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:E5, constructed from sample accession ERS1903658 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903658">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903658</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278680</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#5" accession="ERX2663268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:H5, constructed from sample accession ERS1903661 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903661">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903661</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278683</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#16" accession="ERX2663269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D7, constructed from sample accession ERS1903673 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903673">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903673</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#19" accession="ERX2663270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:G7, constructed from sample accession ERS1903676 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903676">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903676</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#22" accession="ERX2663271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:B8, constructed from sample accession ERS1903679 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903679">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903679</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#25" accession="ERX2663272">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:E8, constructed from sample accession ERS1903682 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903682">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903682</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#28" accession="ERX2663273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:A9, constructed from sample accession ERS1903686 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903686">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903686</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_1#31" accession="ERX2663274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D9, constructed from sample accession ERS1903689 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903689">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903689</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278711</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#1" accession="ERX2663275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D5, constructed from sample accession ERS1903657 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903657">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903657</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278679</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="370" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#4" accession="ERX2663276">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:G5, constructed from sample accession ERS1903660 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903660">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903660</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278682</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="359" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#15" accession="ERX2663277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C7, constructed from sample accession ERS1903672 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903672">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903672</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#18" accession="ERX2663278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:F7, constructed from sample accession ERS1903675 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903675">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903675</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#21" accession="ERX2663279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:A8, constructed from sample accession ERS1903678 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903678">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903678</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#24" accession="ERX2663280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:D8, constructed from sample accession ERS1903681 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903681">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903681</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="120"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#27" accession="ERX2663281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:H8, constructed from sample accession ERS1903685 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903685">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903685</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278707</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#30" accession="ERX2663282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C9, constructed from sample accession ERS1903688 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903688">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903688</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_2#33" accession="ERX2663283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:F9, constructed from sample accession ERS1903691 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_2).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903691">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903691</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278713</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#3" accession="ERX2663284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:F5, constructed from sample accession ERS1903659 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903659">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903659</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278681</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#14" accession="ERX2663285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:B7, constructed from sample accession ERS1903671 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903671">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903671</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#17" accession="ERX2663286">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:E7, constructed from sample accession ERS1903674 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903674">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903674</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#20" accession="ERX2663287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:H7, constructed from sample accession ERS1903677 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903677">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903677</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#23" accession="ERX2663288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:C8, constructed from sample accession ERS1903680 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903680">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903680</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#26" accession="ERX2663289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:F8, constructed from sample accession ERS1903683 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903683">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903683</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#29" accession="ERX2663290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:B9, constructed from sample accession ERS1903687 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903687">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903687</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_3#32" accession="ERX2663291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495250S:E9, constructed from sample accession ERS1903690 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_3).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903690">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903690</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278712</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495250S:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#2" accession="ERX2663292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B1, constructed from sample accession ERS1903693 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903693">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903693</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278715</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#5" accession="ERX2663293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E1, constructed from sample accession ERS1903696 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903696">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903696</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278718</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#13" accession="ERX2663294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E2, constructed from sample accession ERS1903704 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903704">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903704</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#16" accession="ERX2663295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:H2, constructed from sample accession ERS1903707 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903707">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903707</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#19" accession="ERX2663296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:C3, constructed from sample accession ERS1903710 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903710">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903710</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#22" accession="ERX2663297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F3, constructed from sample accession ERS1903713 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903713">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903713</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#25" accession="ERX2663298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:A4, constructed from sample accession ERS1903716 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903716">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903716</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#28" accession="ERX2663299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:D4, constructed from sample accession ERS1903719 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903719">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903719</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#31" accession="ERX2663300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:G4, constructed from sample accession ERS1903722 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903722">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903722</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_4#34" accession="ERX2663301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_4#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_4#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B5, constructed from sample accession ERS1903725 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_4).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903725">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903725</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#2" accession="ERX2663302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B1, constructed from sample accession ERS1903693 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903693">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903693</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278715</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#10" accession="ERX2663303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B2, constructed from sample accession ERS1903701 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903701">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903701</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#13" accession="ERX2663304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E2, constructed from sample accession ERS1903704 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903704">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903704</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#16" accession="ERX2663305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:H2, constructed from sample accession ERS1903707 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903707">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903707</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#19" accession="ERX2663306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:C3, constructed from sample accession ERS1903710 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903710">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903710</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#22" accession="ERX2663307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F3, constructed from sample accession ERS1903713 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903713">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903713</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#25" accession="ERX2663308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:A4, constructed from sample accession ERS1903716 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903716">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903716</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#28" accession="ERX2663309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:D4, constructed from sample accession ERS1903719 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903719">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903719</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#31" accession="ERX2663310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:G4, constructed from sample accession ERS1903722 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903722">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903722</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_5#34" accession="ERX2663311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_5#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_5#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B5, constructed from sample accession ERS1903725 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_5).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903725">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903725</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#7" accession="ERX2663312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:G1, constructed from sample accession ERS1903698 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903698">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903698</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278720</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#10" accession="ERX2663313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B2, constructed from sample accession ERS1903701 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903701">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903701</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#13" accession="ERX2663314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E2, constructed from sample accession ERS1903704 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903704">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903704</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278726</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#16" accession="ERX2663315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:H2, constructed from sample accession ERS1903707 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903707">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903707</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278729</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#19" accession="ERX2663316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:C3, constructed from sample accession ERS1903710 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903710">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903710</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278732</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#22" accession="ERX2663317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F3, constructed from sample accession ERS1903713 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903713">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903713</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#25" accession="ERX2663318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:A4, constructed from sample accession ERS1903716 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903716">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903716</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#28" accession="ERX2663319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:D4, constructed from sample accession ERS1903719 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903719">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903719</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_6#31" accession="ERX2663320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_6#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_6#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:G4, constructed from sample accession ERS1903722 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_6).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903722">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903722</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#4" accession="ERX2663321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:D1, constructed from sample accession ERS1903765 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903765">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#7" accession="ERX2663322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:G1, constructed from sample accession ERS1903768 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903768">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#10" accession="ERX2663323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B2, constructed from sample accession ERS1903771 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903771">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#13" accession="ERX2663324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E2, constructed from sample accession ERS1903774 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903774">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#16" accession="ERX2663325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:H2, constructed from sample accession ERS1903777 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903777">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#19" accession="ERX2663326">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C3, constructed from sample accession ERS1903780 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903780">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#22" accession="ERX2663327">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F3, constructed from sample accession ERS1903783 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903783">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#25" accession="ERX2663328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B4, constructed from sample accession ERS1903787 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903787">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_7#28" accession="ERX2663329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E4, constructed from sample accession ERS1903790 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903790">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903790</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#2" accession="ERX2663330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B1, constructed from sample accession ERS1903763 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903763">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903763</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#5" accession="ERX2663331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E1, constructed from sample accession ERS1903766 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903766">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903766</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#8" accession="ERX2663332">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:H1, constructed from sample accession ERS1903769 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903769">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903769</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#11" accession="ERX2663333">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C2, constructed from sample accession ERS1903772 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903772">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903772</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#14" accession="ERX2663334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F2, constructed from sample accession ERS1903775 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903775">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903775</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#17" accession="ERX2663335">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:A3, constructed from sample accession ERS1903778 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903778">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903778</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#20" accession="ERX2663336">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:D3, constructed from sample accession ERS1903781 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903781">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903781</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#23" accession="ERX2663337">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:G3, constructed from sample accession ERS1903784 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903784">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903784</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#26" accession="ERX2663338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C4, constructed from sample accession ERS1903788 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903788">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903788</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24186_8#34" accession="ERX2663339">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24186_8#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24186_8#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C5, constructed from sample accession ERS1903796 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24186_8).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903796">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903796</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#3" accession="ERX2663340">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F5, constructed from sample accession ERS1903799 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903799">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#6" accession="ERX2663341">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:A6, constructed from sample accession ERS1903802 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903802">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#9" accession="ERX2663342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:D6, constructed from sample accession ERS1903805 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903805">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#12" accession="ERX2663343">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:G6, constructed from sample accession ERS1903808 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903808">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#15" accession="ERX2663344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B7, constructed from sample accession ERS1903811 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903811">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#18" accession="ERX2663345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E7, constructed from sample accession ERS1903814 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="342" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#21" accession="ERX2663346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:H7, constructed from sample accession ERS1903817 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903817">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903817</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#32" accession="ERX2663347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C9, constructed from sample accession ERS1903828 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_1#35" accession="ERX2663348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F9, constructed from sample accession ERS1903831 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#3" accession="ERX2663349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F5, constructed from sample accession ERS1903799 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903799">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903799</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#6" accession="ERX2663350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:A6, constructed from sample accession ERS1903802 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903802">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903802</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="373" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#9" accession="ERX2663351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:D6, constructed from sample accession ERS1903805 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903805">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903805</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#12" accession="ERX2663352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:G6, constructed from sample accession ERS1903808 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903808">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903808</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#15" accession="ERX2663353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B7, constructed from sample accession ERS1903811 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903811">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903811</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#18" accession="ERX2663354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E7, constructed from sample accession ERS1903814 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903814">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903814</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="340" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#29" accession="ERX2663355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:H8, constructed from sample accession ERS1903825 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903825">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#32" accession="ERX2663356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C9, constructed from sample accession ERS1903828 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903828">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_2#35" accession="ERX2663357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F9, constructed from sample accession ERS1903831 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_2).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903831">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#3" accession="ERX2663358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:F5, constructed from sample accession ERS1903939 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903939">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903939</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#6" accession="ERX2663359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A6, constructed from sample accession ERS1903942 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#9" accession="ERX2663360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:D6, constructed from sample accession ERS1903945 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#12" accession="ERX2663361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:G6, constructed from sample accession ERS1903948 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#15" accession="ERX2663362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:B7, constructed from sample accession ERS1903951 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#26" accession="ERX2663363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:E8, constructed from sample accession ERS1903962 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903962">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903962</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#29" accession="ERX2663364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:H8, constructed from sample accession ERS1903965 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903965">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903965</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_3#32" accession="ERX2663365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:C9, constructed from sample accession ERS1903968 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_3).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#1" accession="ERX2663366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:D5, constructed from sample accession ERS1903937 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903937">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903937</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278959</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#4" accession="ERX2663367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:G5, constructed from sample accession ERS1903940 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903940">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903940</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#7" accession="ERX2663368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:B6, constructed from sample accession ERS1903943 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#10" accession="ERX2663369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:E6, constructed from sample accession ERS1903946 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#13" accession="ERX2663370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:H6, constructed from sample accession ERS1903949 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#24" accession="ERX2663371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:C8, constructed from sample accession ERS1903960 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903960">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903960</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#27" accession="ERX2663372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:F8, constructed from sample accession ERS1903963 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#30" accession="ERX2663373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A9, constructed from sample accession ERS1903966 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903966">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903966</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="388" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_4#33" accession="ERX2663374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_4#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_4#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:D9, constructed from sample accession ERS1903969 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_4).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903969">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903969</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="353" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#2" accession="ERX2663375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:E5, constructed from sample accession ERS1903938 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903938">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903938</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#5" accession="ERX2663376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:H5, constructed from sample accession ERS1903941 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#8" accession="ERX2663377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:C6, constructed from sample accession ERS1903944 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#11" accession="ERX2663378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:F6, constructed from sample accession ERS1903947 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#22" accession="ERX2663379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A8, constructed from sample accession ERS1903958 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="381" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#25" accession="ERX2663380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:D8, constructed from sample accession ERS1903961 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="121"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#28" accession="ERX2663381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:G8, constructed from sample accession ERS1903964 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903964">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903964</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#31" accession="ERX2663382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:B9, constructed from sample accession ERS1903967 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903967">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903967</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_5#34" accession="ERX2663383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_5#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_5#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:F9, constructed from sample accession ERS1903971 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_5).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903971">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903971</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#3" accession="ERX2663384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C1, constructed from sample accession ERS1903974 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#6" accession="ERX2663385">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:F1, constructed from sample accession ERS1903977 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="356" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#9" accession="ERX2663386">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:A2, constructed from sample accession ERS1903980 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#20" accession="ERX2663387">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D3, constructed from sample accession ERS1903991 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#23" accession="ERX2663388">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:G3, constructed from sample accession ERS1903994 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#26" accession="ERX2663389">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:B4, constructed from sample accession ERS1903997 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#29" accession="ERX2663390">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:E4, constructed from sample accession ERS1904015 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#32" accession="ERX2663391">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:H4, constructed from sample accession ERS1904018 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_6#35" accession="ERX2663392">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_6#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_6#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C5, constructed from sample accession ERS1904021 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_6).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#3" accession="ERX2663393">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C1, constructed from sample accession ERS1903974 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#6" accession="ERX2663394">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:F1, constructed from sample accession ERS1903977 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="353" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#9" accession="ERX2663395">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:A2, constructed from sample accession ERS1903980 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903980">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903980</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#17" accession="ERX2663396">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:A3, constructed from sample accession ERS1903988 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#20" accession="ERX2663397">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D3, constructed from sample accession ERS1903991 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#23" accession="ERX2663398">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:G3, constructed from sample accession ERS1903994 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#26" accession="ERX2663399">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:B4, constructed from sample accession ERS1903997 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#29" accession="ERX2663400">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:E4, constructed from sample accession ERS1904015 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#32" accession="ERX2663401">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:H4, constructed from sample accession ERS1904018 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_7#35" accession="ERX2663402">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_7#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_7#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C5, constructed from sample accession ERS1904021 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_7).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#3" accession="ERX2663403">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C1, constructed from sample accession ERS1903974 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903974">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903974</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="373" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#6" accession="ERX2663404">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:F1, constructed from sample accession ERS1903977 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903977">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903977</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="359" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#14" accession="ERX2663405">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:F2, constructed from sample accession ERS1903985 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279007</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#17" accession="ERX2663406">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:A3, constructed from sample accession ERS1903988 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279010</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#20" accession="ERX2663407">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:D3, constructed from sample accession ERS1903991 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#23" accession="ERX2663408">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:G3, constructed from sample accession ERS1903994 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279016</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#26" accession="ERX2663409">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:B4, constructed from sample accession ERS1903997 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903997">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903997</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279019</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#29" accession="ERX2663410">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:E4, constructed from sample accession ERS1904015 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904015">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904015</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="405" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#32" accession="ERX2663411">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:H4, constructed from sample accession ERS1904018 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904018">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904018</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24187_8#35" accession="ERX2663412">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24187_8#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24187_8#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495255A:C5, constructed from sample accession ERS1904021 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24187_8).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904021">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904021</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495255A:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#3" accession="ERX2663413">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C1, constructed from sample accession ERS1903834 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903834">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#11" accession="ERX2663414">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C2, constructed from sample accession ERS1903842 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#14" accession="ERX2663415">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:F2, constructed from sample accession ERS1903845 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#17" accession="ERX2663416">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:A3, constructed from sample accession ERS1903848 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#20" accession="ERX2663417">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:D3, constructed from sample accession ERS1903851 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="422" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#23" accession="ERX2663418">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:G3, constructed from sample accession ERS1903854 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#26" accession="ERX2663419">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:B4, constructed from sample accession ERS1903857 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="423" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#29" accession="ERX2663420">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E4, constructed from sample accession ERS1903860 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="423" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#32" accession="ERX2663421">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H4, constructed from sample accession ERS1903863 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_1#35" accession="ERX2663422">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C5, constructed from sample accession ERS1903866 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903866">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903866</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#8" accession="ERX2663423">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H1, constructed from sample accession ERS1903839 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#11" accession="ERX2663424">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C2, constructed from sample accession ERS1903842 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#14" accession="ERX2663425">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:F2, constructed from sample accession ERS1903845 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#17" accession="ERX2663426">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:A3, constructed from sample accession ERS1903848 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#20" accession="ERX2663427">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:D3, constructed from sample accession ERS1903851 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#23" accession="ERX2663428">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:G3, constructed from sample accession ERS1903854 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#26" accession="ERX2663429">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:B4, constructed from sample accession ERS1903857 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#29" accession="ERX2663430">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E4, constructed from sample accession ERS1903860 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_2#32" accession="ERX2663431">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H4, constructed from sample accession ERS1903863 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_2).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903863">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903863</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#5" accession="ERX2663432">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E1, constructed from sample accession ERS1903836 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903836">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#8" accession="ERX2663433">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H1, constructed from sample accession ERS1903839 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903839">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="414" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#11" accession="ERX2663434">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C2, constructed from sample accession ERS1903842 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903842">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#14" accession="ERX2663435">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:F2, constructed from sample accession ERS1903845 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903845">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#17" accession="ERX2663436">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:A3, constructed from sample accession ERS1903848 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903848">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#20" accession="ERX2663437">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:D3, constructed from sample accession ERS1903851 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903851">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903851</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="423" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#23" accession="ERX2663438">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:G3, constructed from sample accession ERS1903854 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903854">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903854</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#26" accession="ERX2663439">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:B4, constructed from sample accession ERS1903857 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903857">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903857</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="423" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_3#29" accession="ERX2663440">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E4, constructed from sample accession ERS1903860 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_3).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903860">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903860</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#2" accession="ERX2663441">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:B1, constructed from sample accession ERS1904043 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#5" accession="ERX2663442">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:E1, constructed from sample accession ERS1904046 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#8" accession="ERX2663443">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:H1, constructed from sample accession ERS1904049 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="401" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#11" accession="ERX2663444">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:C2, constructed from sample accession ERS1904052 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#14" accession="ERX2663445">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:F2, constructed from sample accession ERS1904055 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279077</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#17" accession="ERX2663446">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A3, constructed from sample accession ERS1904058 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904058">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#20" accession="ERX2663447">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:E3, constructed from sample accession ERS1904062 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904062">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904062</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="357" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#23" accession="ERX2663448">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A4, constructed from sample accession ERS1904066 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904066">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904066</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="324" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_4#26" accession="ERX2663449">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_4#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_4#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:G4, constructed from sample accession ERS1904072 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_4).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904072">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904072</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279094</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#6" accession="ERX2663450">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:F1, constructed from sample accession ERS1904047 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904047">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904047</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#9" accession="ERX2663451">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A2, constructed from sample accession ERS1904050 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904050">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904050</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279072</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#12" accession="ERX2663452">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:D2, constructed from sample accession ERS1904053 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279075</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#15" accession="ERX2663453">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:G2, constructed from sample accession ERS1904056 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279078</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#21" accession="ERX2663455">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:F3, constructed from sample accession ERS1904063 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904063">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904063</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279085</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#24" accession="ERX2663456">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:D4, constructed from sample accession ERS1904069 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904069">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="337" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#27" accession="ERX2663457">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A5, constructed from sample accession ERS1904074 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904074">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904074</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279096</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="370" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#10" accession="ERX2663458">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:E6, constructed from sample accession ERS1904086 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="363" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#13" accession="ERX2663459">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:H6, constructed from sample accession ERS1904089 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904089">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904089</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#16" accession="ERX2663460">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663460</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:C7, constructed from sample accession ERS1904092 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904092">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904092</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="351" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#19" accession="ERX2663461">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663461</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:F7, constructed from sample accession ERS1904095 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904095">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904095</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="355" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#22" accession="ERX2663462">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663462</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A8, constructed from sample accession ERS1904098 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="335" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#25" accession="ERX2663463">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663463</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:E8, constructed from sample accession ERS1904102 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904102">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904102</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#28" accession="ERX2663464">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663464</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:H8, constructed from sample accession ERS1904105 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_6#31" accession="ERX2663465">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663465</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_6#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_6#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:C9, constructed from sample accession ERS1904108 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_6).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="342" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#8" accession="ERX2663466">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663466</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:C6, constructed from sample accession ERS1904084 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#11" accession="ERX2663467">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663467</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:F6, constructed from sample accession ERS1904087 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="348" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#14" accession="ERX2663468">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663468</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A7, constructed from sample accession ERS1904090 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904090">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904090</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#17" accession="ERX2663469">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663469</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:D7, constructed from sample accession ERS1904093 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904093">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904093</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="337" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#20" accession="ERX2663470">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663470</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:G7, constructed from sample accession ERS1904096 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904096">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904096</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="354" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#23" accession="ERX2663471">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663471</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:B8, constructed from sample accession ERS1904099 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904099">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904099</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="363" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#26" accession="ERX2663472">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663472</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:F8, constructed from sample accession ERS1904103 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904103">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904103</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="373" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_7#29" accession="ERX2663473">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663473</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A9, constructed from sample accession ERS1904106 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_7).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="351" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#6" accession="ERX2663474">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663474</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A6, constructed from sample accession ERS1904082 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904082">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#9" accession="ERX2663475">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663475</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:D6, constructed from sample accession ERS1904085 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="358" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#12" accession="ERX2663476">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663476</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:G6, constructed from sample accession ERS1904088 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904088">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#15" accession="ERX2663477">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663477</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:B7, constructed from sample accession ERS1904091 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904091">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904091</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="358" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#18" accession="ERX2663478">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663478</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:E7, constructed from sample accession ERS1904094 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904094">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904094</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#21" accession="ERX2663479">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663479</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:H7, constructed from sample accession ERS1904097 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#24" accession="ERX2663480">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663480</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:C8, constructed from sample accession ERS1904100 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904100">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904100</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_8#27" accession="ERX2663481">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663481</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_8#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_8#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:G8, constructed from sample accession ERS1904104 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_8).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904104">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904104</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="354" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#4" accession="ERX2663482">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663482</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:D1, constructed from sample accession ERS1903765 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903765">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903765</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#7" accession="ERX2663483">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663483</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:G1, constructed from sample accession ERS1903768 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903768">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903768</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#10" accession="ERX2663484">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663484</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B2, constructed from sample accession ERS1903771 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903771">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903771</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#13" accession="ERX2663485">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663485</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E2, constructed from sample accession ERS1903774 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903774">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903774</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#16" accession="ERX2663486">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:H2, constructed from sample accession ERS1903777 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903777">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903777</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#19" accession="ERX2663487">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C3, constructed from sample accession ERS1903780 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903780">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903780</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#22" accession="ERX2663488">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F3, constructed from sample accession ERS1903783 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903783">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903783</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_1#25" accession="ERX2663489">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B4, constructed from sample accession ERS1903787 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903787">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903787</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#2" accession="ERX2663490">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E5, constructed from sample accession ERS1903798 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903798">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903798</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="398" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#5" accession="ERX2663491">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:H5, constructed from sample accession ERS1903801 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903801">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903801</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#8" accession="ERX2663492">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:C6, constructed from sample accession ERS1903804 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903804">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903804</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#11" accession="ERX2663493">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:F6, constructed from sample accession ERS1903807 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903807">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903807</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#14" accession="ERX2663494">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:A7, constructed from sample accession ERS1903810 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903810">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903810</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#17" accession="ERX2663495">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:D7, constructed from sample accession ERS1903813 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903813">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903813</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#20" accession="ERX2663496">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:G7, constructed from sample accession ERS1903816 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903816">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903816</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#23" accession="ERX2663497">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:B8, constructed from sample accession ERS1903819 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903819">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903819</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#26" accession="ERX2663498">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E8, constructed from sample accession ERS1903822 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903822">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903822</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_2#34" accession="ERX2663499">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495252U:E9, constructed from sample accession ERS1903830 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_2).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903830">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495252U:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#2" accession="ERX2663500">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:B1, constructed from sample accession ERS1904043 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904043">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904043</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#5" accession="ERX2663501">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:E1, constructed from sample accession ERS1904046 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904046">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904046</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#8" accession="ERX2663502">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:H1, constructed from sample accession ERS1904049 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904049">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904049</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279071</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#11" accession="ERX2663503">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:C2, constructed from sample accession ERS1904052 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279074</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#14" accession="ERX2663504">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:F2, constructed from sample accession ERS1904055 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279077</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#17" accession="ERX2663505">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A3, constructed from sample accession ERS1904058 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904058">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#20" accession="ERX2663506">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:E3, constructed from sample accession ERS1904062 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904062">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904062</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279084</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="354" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_3#23" accession="ERX2663507">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:A4, constructed from sample accession ERS1904066 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_3).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904066">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904066</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#3" accession="ERX2663508">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:F5, constructed from sample accession ERS1904149 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904149">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#6" accession="ERX2663509">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:A6, constructed from sample accession ERS1904152 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904152">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#9" accession="ERX2663510">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D6, constructed from sample accession ERS1904155 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904155">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#12" accession="ERX2663511">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:G6, constructed from sample accession ERS1904158 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904158">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#15" accession="ERX2663512">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:B7, constructed from sample accession ERS1904161 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904161">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#18" accession="ERX2663513">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:E7, constructed from sample accession ERS1904164 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#21" accession="ERX2663514">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:H7, constructed from sample accession ERS1904167 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904167">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#24" accession="ERX2663515">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:C8, constructed from sample accession ERS1904170 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904170">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#27" accession="ERX2663516">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:F8, constructed from sample accession ERS1904173 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904173">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_4#35" accession="ERX2663517">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_4#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_4#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:F9, constructed from sample accession ERS1904181 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_4).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904181">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904181</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279203</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#3" accession="ERX2663518">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F5, constructed from sample accession ERS1904289 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279311</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#6" accession="ERX2663519">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:A6, constructed from sample accession ERS1904292 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904292">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279314</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#12" accession="ERX2663521">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:G6, constructed from sample accession ERS1904298 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904298">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279320</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="451" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#15" accession="ERX2663522">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:B7, constructed from sample accession ERS1904301 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#21" accession="ERX2663524">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:H7, constructed from sample accession ERS1904307 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904307">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#24" accession="ERX2663525">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:C8, constructed from sample accession ERS1904310 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904310">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279332</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#35" accession="ERX2663527">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:F9, constructed from sample accession ERS1904321 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279343</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_6#3" accession="ERX2663528">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A3, constructed from sample accession ERS1888097 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_6).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888097">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888097</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229079</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="24"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_6#9" accession="ERX2663530">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D1, constructed from sample accession ERS1888083 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_6).  This submission includes reads tagged with the sequence CCGAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888083">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="208" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_6#12" accession="ERX2663531">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E1, constructed from sample accession ERS1888084 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_6).  This submission includes reads tagged with the sequence GATAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="182"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_6#18" accession="ERX2663533">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G1, constructed from sample accession ERS1888086 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_6).  This submission includes reads tagged with the sequence AATGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="303" NOMINAL_SDEV="186"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_6#21" accession="ERX2663534">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H1, constructed from sample accession ERS1888087 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_6).  This submission includes reads tagged with the sequence CCATCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_7#9" accession="ERX2663536">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D1, constructed from sample accession ERS1888083 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_7).  This submission includes reads tagged with the sequence CCGAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888083">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888083</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="207" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_7#12" accession="ERX2663537">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E1, constructed from sample accession ERS1888084 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_7).  This submission includes reads tagged with the sequence GATAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888084">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888084</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_7#18" accession="ERX2663539">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G1, constructed from sample accession ERS1888086 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_7).  This submission includes reads tagged with the sequence AATGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301" NOMINAL_SDEV="199"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_7#21" accession="ERX2663540">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H1, constructed from sample accession ERS1888087 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_7).  This submission includes reads tagged with the sequence CCATCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="165"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_8#4" accession="ERX2663542">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B1, constructed from sample accession ERS1888081 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_8).  This submission includes reads tagged with the sequence AACAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888081">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888081</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_8#7" accession="ERX2663543">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C1, constructed from sample accession ERS1888082 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_8).  This submission includes reads tagged with the sequence AGATCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888082">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888082</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="199" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_8#18" accession="ERX2663545">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G1, constructed from sample accession ERS1888086 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_8).  This submission includes reads tagged with the sequence AATGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888086">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888086</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="247" NOMINAL_SDEV="169"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_8#21" accession="ERX2663546">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H1, constructed from sample accession ERS1888087 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_8).  This submission includes reads tagged with the sequence CCATCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888087">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888087</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_1#4" accession="ERX2663548">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B4, constructed from sample accession ERS1888106 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_1).  This submission includes reads tagged with the sequence AAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="187" NOMINAL_SDEV="20"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_1#7" accession="ERX2663549">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C4, constructed from sample accession ERS1888107 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_1).  This submission includes reads tagged with the sequence ATCCTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888107">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="319"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_1#13" accession="ERX2663551">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E4, constructed from sample accession ERS1888109 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_1).  This submission includes reads tagged with the sequence GCTAACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_1#16" accession="ERX2663552">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F5, constructed from sample accession ERS1888119 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_1).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="186" NOMINAL_SDEV="60"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#4" accession="ERX2663554">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B4, constructed from sample accession ERS1888106 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence AAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888106">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888106</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229088</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="190" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#7" accession="ERX2663555">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C4, constructed from sample accession ERS1888107 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence ATCCTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888107">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888107</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229089</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="272" NOMINAL_SDEV="114"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#13" accession="ERX2663557">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E4, constructed from sample accession ERS1888109 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence GCTAACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#16" accession="ERX2663558">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F5, constructed from sample accession ERS1888119 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#22" accession="ERX2663560">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H5, constructed from sample accession ERS1888121 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_3#10" accession="ERX2663561">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D4, constructed from sample accession ERS1888108 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_3).  This submission includes reads tagged with the sequence CGAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229090</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_3#16" accession="ERX2663563">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F5, constructed from sample accession ERS1888119 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_3).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="183" NOMINAL_SDEV="15"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_3#19" accession="ERX2663564">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G5, constructed from sample accession ERS1888120 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_3).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="271" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_4#2" accession="ERX2663566">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A8, constructed from sample accession ERS1888144 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_4).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888144">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="198" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_4#5" accession="ERX2663567">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B8, constructed from sample accession ERS1888145 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_4).  This submission includes reads tagged with the sequence ACCTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888145">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="27"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_4#19" accession="ERX2663569">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G7, constructed from sample accession ERS1888138 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_4).  This submission includes reads tagged with the sequence AGGCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888138">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="181" NOMINAL_SDEV="16"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_4#22" accession="ERX2663570">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H7, constructed from sample accession ERS1888143 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_4).  This submission includes reads tagged with the sequence CTAAGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888143">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_5#4" accession="ERX2663572">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B7, constructed from sample accession ERS1888133 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_5).  This submission includes reads tagged with the sequence ACAGCAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888133">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="284" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_5#7" accession="ERX2663573">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C7, constructed from sample accession ERS1888134 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_5).  This submission includes reads tagged with the sequence GACTAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="179" NOMINAL_SDEV="12"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_5#13" accession="ERX2663575">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E7, constructed from sample accession ERS1888136 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_5).  This submission includes reads tagged with the sequence GGTGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="180" NOMINAL_SDEV="27"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_5#16" accession="ERX2663576">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F7, constructed from sample accession ERS1888137 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_5).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="163" NOMINAL_SDEV="1"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#6" accession="ERX2663578">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B9, constructed from sample accession ERS1888158 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence ACGCTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888158">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="459" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#9" accession="ERX2663579">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C9, constructed from sample accession ERS1888159 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence CACTTCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888159">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="195" NOMINAL_SDEV="60"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#15" accession="ERX2663581">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E9, constructed from sample accession ERS1888165 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence GTCGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888165">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888165</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#18" accession="ERX2663582">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F9, constructed from sample accession ERS1888166 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence AACTCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888166">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888166</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#24" accession="ERX2663584">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H9, constructed from sample accession ERS1888169 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence GACAGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888169">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888169</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="183" NOMINAL_SDEV="24"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_7#11" accession="ERX2663585">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D11, constructed from sample accession ERS1888187 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_7).  This submission includes reads tagged with the sequence CAAGACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888187">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="207" NOMINAL_SDEV="147"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_7#17" accession="ERX2663587">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663587</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F11, constructed from sample accession ERS1888190 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_7).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888190">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888190</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="163" NOMINAL_SDEV="2"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24188_5#18" accession="ERX2663454">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24188_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24188_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495268F:C3, constructed from sample accession ERS1904060 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24188_5).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904060">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904060</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279082</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495268F:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="370" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#9" accession="ERX2663520">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:D6, constructed from sample accession ERS1904295 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904295">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279317</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#18" accession="ERX2663523">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:E7, constructed from sample accession ERS1904304 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279326</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_5#32" accession="ERX2663526">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_5#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_5#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495271A:C9, constructed from sample accession ERS1904318 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_5).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904318">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495271A:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_6#6" accession="ERX2663529">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B3, constructed from sample accession ERS1888098 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_6).  This submission includes reads tagged with the sequence AACGCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="164"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_6#15" accession="ERX2663532">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F1, constructed from sample accession ERS1888085 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_6).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="205" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_7#6" accession="ERX2663535">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B3, constructed from sample accession ERS1888098 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_7).  This submission includes reads tagged with the sequence AACGCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888098">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888098</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229080</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="149"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_7#15" accession="ERX2663538">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F1, constructed from sample accession ERS1888085 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_7).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="215" NOMINAL_SDEV="25"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_8#1" accession="ERX2663541">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A1, constructed from sample accession ERS1888080 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_8).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888080">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888080</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="154"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24196_8#15" accession="ERX2663544">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24196_8#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24196_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F1, constructed from sample accession ERS1888085 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24196_8).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888085">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888085</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="184" NOMINAL_SDEV="37"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_1#1" accession="ERX2663547">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A4, constructed from sample accession ERS1888105 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_1).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="10"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_1#10" accession="ERX2663550">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D4, constructed from sample accession ERS1888108 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_1).  This submission includes reads tagged with the sequence CGAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229090</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="323" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#1" accession="ERX2663553">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A4, constructed from sample accession ERS1888105 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888105">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888105</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229087</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#10" accession="ERX2663556">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D4, constructed from sample accession ERS1888108 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence CGAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888108">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888108</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229090</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="164" NOMINAL_SDEV="10"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_2#19" accession="ERX2663559">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G5, constructed from sample accession ERS1888120 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_2).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_3#13" accession="ERX2663562">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E4, constructed from sample accession ERS1888109 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_3).  This submission includes reads tagged with the sequence GCTAACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888109">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888109</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229091</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_3#22" accession="ERX2663565">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H5, constructed from sample accession ERS1888121 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_3).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_4#8" accession="ERX2663568">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C8, constructed from sample accession ERS1888148 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_4).  This submission includes reads tagged with the sequence CAATGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888148">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_5#1" accession="ERX2663571">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A7, constructed from sample accession ERS1888130 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="190"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_5#10" accession="ERX2663574">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D7, constructed from sample accession ERS1888135 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_5).  This submission includes reads tagged with the sequence CTCAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="197" NOMINAL_SDEV="28"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#3" accession="ERX2663577">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A9, constructed from sample accession ERS1888157 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence CGCTGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888157">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="191" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#12" accession="ERX2663580">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D9, constructed from sample accession ERS1888164 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence CTGGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="224"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_6#21" accession="ERX2663583">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G9, constructed from sample accession ERS1888168 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_6).  This submission includes reads tagged with the sequence ATCATTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888168">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_7#14" accession="ERX2663586">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663586</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E11, constructed from sample accession ERS1888188 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_7).  This submission includes reads tagged with the sequence GTGTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888188">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_7#20" accession="ERX2663588">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663588</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G11, constructed from sample accession ERS1888191 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_7).  This submission includes reads tagged with the sequence CAAGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888191">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="162" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_7#23" accession="ERX2663589">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663589</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H11, constructed from sample accession ERS1888192 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_7).  This submission includes reads tagged with the sequence GATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888192">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888192</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_8#2" accession="ERX2663590">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663590</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A11, constructed from sample accession ERS1888182 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_8).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888182">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888182</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="42"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_8#5" accession="ERX2663591">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663591</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B11, constructed from sample accession ERS1888185 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_8).  This submission includes reads tagged with the sequence ACTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888185">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="182" NOMINAL_SDEV="19"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_8#8" accession="ERX2663592">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663592</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C11, constructed from sample accession ERS1888186 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_8).  This submission includes reads tagged with the sequence CATACCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888186">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_8#19" accession="ERX2663593">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663593</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:G10, constructed from sample accession ERS1888177 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_8).  This submission includes reads tagged with the sequence ATTGGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888177">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24197_8#22" accession="ERX2663594">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663594</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24197_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24197_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H10, constructed from sample accession ERS1888179 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24197_8).  This submission includes reads tagged with the sequence GAGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888179">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="184" NOMINAL_SDEV="17"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#1" accession="ERX2663595">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663595</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A1, constructed from sample accession ERS1903902 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#4" accession="ERX2663596">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663596</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:D1, constructed from sample accession ERS1903905 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#7" accession="ERX2663597">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663597</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:G1, constructed from sample accession ERS1903908 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#10" accession="ERX2663598">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663598</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:B2, constructed from sample accession ERS1903911 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#13" accession="ERX2663599">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663599</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:E2, constructed from sample accession ERS1903914 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#16" accession="ERX2663600">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663600</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:H2, constructed from sample accession ERS1903917 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#19" accession="ERX2663601">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663601</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:C3, constructed from sample accession ERS1903920 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903920">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903920</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#27" accession="ERX2663602">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663602</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:C4, constructed from sample accession ERS1903928 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#30" accession="ERX2663603">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:F4, constructed from sample accession ERS1903931 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="417" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_1#33" accession="ERX2663604">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A5, constructed from sample accession ERS1903934 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_2#1" accession="ERX2663605">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:A10, constructed from sample accession ERS1888171 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_2).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888171">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888171</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_2#4" accession="ERX2663606">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:B10, constructed from sample accession ERS1888172 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_2).  This submission includes reads tagged with the sequence ACGTATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888172">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_2#7" accession="ERX2663607">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:C10, constructed from sample accession ERS1888173 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_2).  This submission includes reads tagged with the sequence CAGCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888173">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="296" NOMINAL_SDEV="164"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_2#10" accession="ERX2663608">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:D10, constructed from sample accession ERS1888174 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_2).  This submission includes reads tagged with the sequence GAATCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888174">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_2#13" accession="ERX2663609">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663609</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:E10, constructed from sample accession ERS1888175 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_2).  This submission includes reads tagged with the sequence GTCTGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888175">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="911" NOMINAL_SDEV="722"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_2#16" accession="ERX2663610">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663610</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:F10, constructed from sample accession ERS1888176 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_2).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888176">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="193"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_2#24" accession="ERX2663611">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663611</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495717J:H12, constructed from sample accession ERS1888200 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_2).  This submission includes reads tagged with the sequence GCCAAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888200">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888200</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495717J:H12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#3" accession="ERX2663612">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663612</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A3, constructed from sample accession ERS1888271 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888271">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229253</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="195" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#6" accession="ERX2663613">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663613</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B3, constructed from sample accession ERS1888273 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence AACGCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888273">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229255</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="177" NOMINAL_SDEV="236"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#9" accession="ERX2663614">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663614</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C3, constructed from sample accession ERS1888274 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence AGTCACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888274">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229256</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="195" NOMINAL_SDEV="51"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#12" accession="ERX2663615">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663615</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D3, constructed from sample accession ERS1888276 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence CCTCCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888276">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229258</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="196" NOMINAL_SDEV="66"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#15" accession="ERX2663616">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663616</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E3, constructed from sample accession ERS1888277 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence GCGAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888277">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229259</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="37"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#18" accession="ERX2663617">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663617</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F3, constructed from sample accession ERS1888255 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888255">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229237</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#21" accession="ERX2663618">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663618</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G3, constructed from sample accession ERS1888256 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence ACAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888256">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888256</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="184" NOMINAL_SDEV="23"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_3#24" accession="ERX2663619">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663619</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H3, constructed from sample accession ERS1888279 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_3).  This submission includes reads tagged with the sequence CCTAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888279">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229261</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="159" NOMINAL_SDEV="4"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_4#8" accession="ERX2663620">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663620</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C2, constructed from sample accession ERS1888259 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_4).  This submission includes reads tagged with the sequence AGCAGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888259">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="339" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_4#11" accession="ERX2663621">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663621</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D2, constructed from sample accession ERS1888263 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_4).  This submission includes reads tagged with the sequence CCGTGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888263">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="188" NOMINAL_SDEV="72"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_4#14" accession="ERX2663622">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663622</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E2, constructed from sample accession ERS1888264 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_4).  This submission includes reads tagged with the sequence GCCACATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888264">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229246</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="181" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_4#17" accession="ERX2663623">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663623</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F2, constructed from sample accession ERS1888265 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_4).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888265">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888265</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229247</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="183" NOMINAL_SDEV="33"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_4#20" accession="ERX2663624">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663624</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G2, constructed from sample accession ERS1888268 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_4).  This submission includes reads tagged with the sequence ACACGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888268">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888268</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229250</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="181" NOMINAL_SDEV="25"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_4#23" accession="ERX2663625">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663625</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H2, constructed from sample accession ERS1888269 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_4).  This submission includes reads tagged with the sequence CCGACAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888269">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_5#2" accession="ERX2663626">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663626</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A2, constructed from sample accession ERS1888250 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_5).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888250">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888250</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="178" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_5#5" accession="ERX2663627">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663627</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B2, constructed from sample accession ERS1888253 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_5).  This submission includes reads tagged with the sequence AACCGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888253">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888253</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="189" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_5#8" accession="ERX2663628">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663628</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C2, constructed from sample accession ERS1888259 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_5).  This submission includes reads tagged with the sequence AGCAGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888259">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229241</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="335" NOMINAL_SDEV="60"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_5#16" accession="ERX2663629">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663629</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F1, constructed from sample accession ERS1888235 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_5).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="188" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_5#19" accession="ERX2663630">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663630</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G1, constructed from sample accession ERS1888239 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_5).  This submission includes reads tagged with the sequence AATGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888239">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888239</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229221</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_5#22" accession="ERX2663631">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H1, constructed from sample accession ERS1888246 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_5).  This submission includes reads tagged with the sequence CCATCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888246">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888246</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_6#1" accession="ERX2663632">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663632</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A4, constructed from sample accession ERS1888280 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_6).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="233" NOMINAL_SDEV="188"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_6#4" accession="ERX2663633">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663633</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B4, constructed from sample accession ERS1888281 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_6).  This submission includes reads tagged with the sequence AAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="330" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_6#7" accession="ERX2663634">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C4, constructed from sample accession ERS1888283 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_6).  This submission includes reads tagged with the sequence ATCCTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888283">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="285"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_6#10" accession="ERX2663635">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D5, constructed from sample accession ERS1888299 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_6).  This submission includes reads tagged with the sequence CGACTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="210" NOMINAL_SDEV="127"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_6#13" accession="ERX2663636">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E5, constructed from sample accession ERS1888300 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_6).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="179" NOMINAL_SDEV="64"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_6#16" accession="ERX2663637">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663637</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F5, constructed from sample accession ERS1888304 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_6).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#1" accession="ERX2663638">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A4, constructed from sample accession ERS1888280 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888280">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229262</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="192" NOMINAL_SDEV="40"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#4" accession="ERX2663639">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:B4, constructed from sample accession ERS1888281 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence AAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888281">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="198"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#7" accession="ERX2663640">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:C4, constructed from sample accession ERS1888283 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence ATCCTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888283">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229265</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="285"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#10" accession="ERX2663641">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D5, constructed from sample accession ERS1888299 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence CGACTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="217" NOMINAL_SDEV="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#13" accession="ERX2663642">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E5, constructed from sample accession ERS1888300 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="69"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#16" accession="ERX2663643">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F5, constructed from sample accession ERS1888304 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#19" accession="ERX2663644">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G5, constructed from sample accession ERS1888315 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_7#22" accession="ERX2663645">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H5, constructed from sample accession ERS1888316 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_7).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229298</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_8#2" accession="ERX2663646">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663646</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:A5, constructed from sample accession ERS1888294 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_8).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888294">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229276</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="199" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_8#10" accession="ERX2663647">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663647</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:D5, constructed from sample accession ERS1888299 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_8).  This submission includes reads tagged with the sequence CGACTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888299">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229281</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="219" NOMINAL_SDEV="130"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_8#13" accession="ERX2663648">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663648</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:E5, constructed from sample accession ERS1888300 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_8).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888300">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229282</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" NOMINAL_SDEV="64"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_8#16" accession="ERX2663649">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663649</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:F5, constructed from sample accession ERS1888304 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_8).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888304">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229286</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="329" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_8#19" accession="ERX2663650">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663650</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:G5, constructed from sample accession ERS1888315 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_8).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888315">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24199_8#22" accession="ERX2663651">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663651</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24199_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24199_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495718K:H5, constructed from sample accession ERS1888316 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24199_8).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888316">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229298</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495718K: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#2" accession="ERX2663652">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663652</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E5, constructed from sample accession ERS1903728 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903728">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903728</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#5" accession="ERX2663653">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663653</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:H5, constructed from sample accession ERS1903731 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903731">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#8" accession="ERX2663654">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663654</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:C6, constructed from sample accession ERS1903734 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903734">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903734</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#11" accession="ERX2663655">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663655</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F6, constructed from sample accession ERS1903737 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903737">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903737</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#19" accession="ERX2663656">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663656</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F7, constructed from sample accession ERS1903745 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903745">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#22" accession="ERX2663657">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663657</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:A8, constructed from sample accession ERS1903748 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903748">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#25" accession="ERX2663658">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663658</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:D8, constructed from sample accession ERS1903751 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903751">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#28" accession="ERX2663659">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663659</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:G8, constructed from sample accession ERS1903754 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903754">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#31" accession="ERX2663660">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663660</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B9, constructed from sample accession ERS1903757 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903757">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_1#34" accession="ERX2663661">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663661</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E9, constructed from sample accession ERS1903760 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903760">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#2" accession="ERX2663662">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663662</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E5, constructed from sample accession ERS1903728 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903728">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903728</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#5" accession="ERX2663663">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663663</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:H5, constructed from sample accession ERS1903731 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903731">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903731</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#16" accession="ERX2663664">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663664</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:C7, constructed from sample accession ERS1903742 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903742">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903742</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#19" accession="ERX2663665">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663665</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F7, constructed from sample accession ERS1903745 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903745">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903745</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#22" accession="ERX2663666">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663666</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:A8, constructed from sample accession ERS1903748 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903748">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903748</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#25" accession="ERX2663667">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663667</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:D8, constructed from sample accession ERS1903751 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903751">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903751</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#28" accession="ERX2663668">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663668</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:G8, constructed from sample accession ERS1903754 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903754">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903754</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#31" accession="ERX2663669">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663669</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B9, constructed from sample accession ERS1903757 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903757">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903757</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_2#34" accession="ERX2663670">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663670</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E9, constructed from sample accession ERS1903760 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_2).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903760">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903760</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#2" accession="ERX2663671">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663671</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:C1, constructed from sample accession ERS1904184 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904184">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279206</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#13" accession="ERX2663672">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663672</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:F2, constructed from sample accession ERS1904195 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904195">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279217</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="358" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#16" accession="ERX2663673">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663673</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:A3, constructed from sample accession ERS1904198 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904198">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904198</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279220</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#19" accession="ERX2663674">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663674</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D3, constructed from sample accession ERS1904201 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904201">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904201</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="370" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#22" accession="ERX2663675">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663675</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:G3, constructed from sample accession ERS1904204 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904204">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904204</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279226</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#25" accession="ERX2663676">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:B4, constructed from sample accession ERS1904207 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904207">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904207</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279229</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#28" accession="ERX2663677">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:E4, constructed from sample accession ERS1904210 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904210">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904210</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279232</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="356" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#31" accession="ERX2663678">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:H4, constructed from sample accession ERS1904213 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904213">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904213</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279235</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_3#34" accession="ERX2663679">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_3#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_3#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:C5, constructed from sample accession ERS1904216 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_3).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904216">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904216</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279238</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="363" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#11" accession="ERX2663680">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D2, constructed from sample accession ERS1904193 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904193">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904193</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279215</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="347" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#14" accession="ERX2663681">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:G2, constructed from sample accession ERS1904196 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904196">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904196</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="386" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#17" accession="ERX2663682">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:B3, constructed from sample accession ERS1904199 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904199">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904199</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279221</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="358" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#20" accession="ERX2663683">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:E3, constructed from sample accession ERS1904202 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904202">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904202</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#23" accession="ERX2663684">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:H3, constructed from sample accession ERS1904205 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904205">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904205</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#26" accession="ERX2663685">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:C4, constructed from sample accession ERS1904208 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904208">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904208</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="373" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#29" accession="ERX2663686">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:F4, constructed from sample accession ERS1904211 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904211">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904211</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_4#32" accession="ERX2663687">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_4#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_4#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:A5, constructed from sample accession ERS1904214 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_4).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904214">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904214</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279236</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#9" accession="ERX2663688">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:B2, constructed from sample accession ERS1904191 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904191">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904191</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#12" accession="ERX2663689">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:E2, constructed from sample accession ERS1904194 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904194">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904194</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279216</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="363" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#15" accession="ERX2663690">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663690</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:H2, constructed from sample accession ERS1904197 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904197">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904197</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279219</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#18" accession="ERX2663691">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663691</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:C3, constructed from sample accession ERS1904200 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904200">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904200</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279222</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#21" accession="ERX2663692">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663692</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:F3, constructed from sample accession ERS1904203 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904203">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904203</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="370" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#24" accession="ERX2663693">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663693</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:A4, constructed from sample accession ERS1904206 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904206">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904206</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279228</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#27" accession="ERX2663694">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663694</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D4, constructed from sample accession ERS1904209 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904209">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904209</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_5#30" accession="ERX2663695">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663695</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_5#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:G4, constructed from sample accession ERS1904212 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_5).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904212">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904212</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#7" accession="ERX2663696">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663696</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:B6, constructed from sample accession ERS1904223 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904223">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#10" accession="ERX2663697">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663697</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:E6, constructed from sample accession ERS1904226 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#13" accession="ERX2663698">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663698</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:H6, constructed from sample accession ERS1904229 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#16" accession="ERX2663699">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:C7, constructed from sample accession ERS1904232 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#19" accession="ERX2663700">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:F7, constructed from sample accession ERS1904235 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#22" accession="ERX2663701">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:A8, constructed from sample accession ERS1904238 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904238">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#25" accession="ERX2663702">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D8, constructed from sample accession ERS1904241 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#28" accession="ERX2663703">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:G8, constructed from sample accession ERS1904244 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="373" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_6#31" accession="ERX2663704">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_6#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_6#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:B9, constructed from sample accession ERS1904247 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_6).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904247">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904247</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279269</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#4" accession="ERX2663705">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663705</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:G5, constructed from sample accession ERS1904220 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279242</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="339" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#7" accession="ERX2663706">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663706</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:B6, constructed from sample accession ERS1904223 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904223">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#10" accession="ERX2663707">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663707</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:E6, constructed from sample accession ERS1904226 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#13" accession="ERX2663708">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663708</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:H6, constructed from sample accession ERS1904229 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#16" accession="ERX2663709">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663709</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:C7, constructed from sample accession ERS1904232 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="363" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#19" accession="ERX2663710">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663710</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:F7, constructed from sample accession ERS1904235 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#22" accession="ERX2663711">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663711</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:A8, constructed from sample accession ERS1904238 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904238">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#25" accession="ERX2663712">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663712</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D8, constructed from sample accession ERS1904241 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_7#28" accession="ERX2663713">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663713</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:G8, constructed from sample accession ERS1904244 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_7).  This submission includes reads tagged with the sequence TGTGAAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279266</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="370" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#1" accession="ERX2663714">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663714</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D5, constructed from sample accession ERS1904217 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904217">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904217</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#4" accession="ERX2663715">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663715</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:G5, constructed from sample accession ERS1904220 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279242</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="339" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#7" accession="ERX2663716">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663716</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:B6, constructed from sample accession ERS1904223 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904223">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904223</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279245</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#10" accession="ERX2663717">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663717</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:E6, constructed from sample accession ERS1904226 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904226">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904226</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="370" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#13" accession="ERX2663718">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663718</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:H6, constructed from sample accession ERS1904229 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279251</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#16" accession="ERX2663719">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663719</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:C7, constructed from sample accession ERS1904232 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904232">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904232</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279254</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="363" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#19" accession="ERX2663720">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663720</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:F7, constructed from sample accession ERS1904235 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904235">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904235</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279257</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#22" accession="ERX2663721">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663721</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:A8, constructed from sample accession ERS1904238 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904238">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904238</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#25" accession="ERX2663722">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663722</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D8, constructed from sample accession ERS1904241 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279263</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24201_8#33" accession="ERX2663723">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663723</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24201_8#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24201_8#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495270W:D9, constructed from sample accession ERS1904249 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24201_8).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904249">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495270W:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="78"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#1" accession="ERX2663724">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663724</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:D5, constructed from sample accession ERS1903867 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903867">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903867</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="436" NOMINAL_SDEV="112"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#4" accession="ERX2663725">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663725</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:G5, constructed from sample accession ERS1903870 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903870">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903870</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#7" accession="ERX2663726">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663726</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:B6, constructed from sample accession ERS1903873 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903873">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903873</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#10" accession="ERX2663727">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663727</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E6, constructed from sample accession ERS1903876 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903876">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903876</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#13" accession="ERX2663728">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663728</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H6, constructed from sample accession ERS1903879 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903879">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903879</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#16" accession="ERX2663729">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663729</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C7, constructed from sample accession ERS1903882 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903882">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903882</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#19" accession="ERX2663730">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663730</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:G7, constructed from sample accession ERS1903886 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903886">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903886</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#22" accession="ERX2663731">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663731</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:B8, constructed from sample accession ERS1903889 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903889">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903889</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#30" accession="ERX2663732">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663732</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:B9, constructed from sample accession ERS1903897 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence TGAAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903897">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903897</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_1#33" accession="ERX2663733">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663733</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E9, constructed from sample accession ERS1903900 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_1).  This submission includes reads tagged with the sequence GGTGAGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903900">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903900</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#2" accession="ERX2663734">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663734</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E5, constructed from sample accession ERS1903868 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903868">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903868</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#5" accession="ERX2663735">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663735</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H5, constructed from sample accession ERS1903871 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903871">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903871</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#8" accession="ERX2663736">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663736</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C6, constructed from sample accession ERS1903874 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903874">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903874</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#11" accession="ERX2663737">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663737</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:F6, constructed from sample accession ERS1903877 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903877">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903877</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:F6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="431" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#14" accession="ERX2663738">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663738</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:A7, constructed from sample accession ERS1903880 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903880">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903880</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#17" accession="ERX2663739">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663739</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:D7, constructed from sample accession ERS1903883 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903883">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903883</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="438" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#20" accession="ERX2663740">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663740</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H7, constructed from sample accession ERS1903887 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903887">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903887</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#28" accession="ERX2663741">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663741</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:H8, constructed from sample accession ERS1903895 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903895">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903895</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="442" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#31" accession="ERX2663742">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:C9, constructed from sample accession ERS1903898 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903898">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903898</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_2#34" accession="ERX2663743">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:F9, constructed from sample accession ERS1903901 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_2).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903901">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903901</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#3" accession="ERX2663744">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:F5, constructed from sample accession ERS1903869 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903869">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903869</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#6" accession="ERX2663745">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:A6, constructed from sample accession ERS1903872 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903872">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903872</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#9" accession="ERX2663746">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:D6, constructed from sample accession ERS1903875 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903875">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903875</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#12" accession="ERX2663747">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:G6, constructed from sample accession ERS1903878 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903878">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903878</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="429" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#15" accession="ERX2663748">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:B7, constructed from sample accession ERS1903881 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903881">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903881</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#18" accession="ERX2663749">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:E7, constructed from sample accession ERS1903884 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903884">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903884</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#26" accession="ERX2663750">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:F8, constructed from sample accession ERS1903893 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903893">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903893</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#29" accession="ERX2663751">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663751</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:A9, constructed from sample accession ERS1903896 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903896">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903896</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="432" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_3#32" accession="ERX2663752">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663752</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495253V:D9, constructed from sample accession ERS1903899 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_3).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903899">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903899</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495253V:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#1" accession="ERX2663753">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663753</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A1, constructed from sample accession ERS1903902 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#4" accession="ERX2663754">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663754</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:D1, constructed from sample accession ERS1903905 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#7" accession="ERX2663755">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663755</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:G1, constructed from sample accession ERS1903908 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#10" accession="ERX2663756">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663756</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:B2, constructed from sample accession ERS1903911 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#13" accession="ERX2663757">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663757</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:E2, constructed from sample accession ERS1903914 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903914">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="116"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#16" accession="ERX2663758">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663758</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:H2, constructed from sample accession ERS1903917 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903917">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="425" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#24" accession="ERX2663759">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663759</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:H3, constructed from sample accession ERS1903925 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#27" accession="ERX2663760">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663760</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:C4, constructed from sample accession ERS1903928 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#30" accession="ERX2663761">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663761</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:F4, constructed from sample accession ERS1903931 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_4#33" accession="ERX2663762">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663762</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_4#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_4#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A5, constructed from sample accession ERS1903934 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_4).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#1" accession="ERX2663763">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663763</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A1, constructed from sample accession ERS1903902 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903902">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903902</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#4" accession="ERX2663764">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663764</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:D1, constructed from sample accession ERS1903905 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903905">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#7" accession="ERX2663765">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663765</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:G1, constructed from sample accession ERS1903908 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903908">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="426" NOMINAL_SDEV="103"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#10" accession="ERX2663766">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663766</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:B2, constructed from sample accession ERS1903911 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903911">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#21" accession="ERX2663767">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663767</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:E3, constructed from sample accession ERS1903922 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903922">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903922</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278944</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#24" accession="ERX2663768">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663768</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:H3, constructed from sample accession ERS1903925 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903925">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903925</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278947</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="422" NOMINAL_SDEV="105"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#27" accession="ERX2663769">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663769</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:C4, constructed from sample accession ERS1903928 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903928">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903928</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#30" accession="ERX2663770">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663770</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:F4, constructed from sample accession ERS1903931 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903931">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903931</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278953</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428" NOMINAL_SDEV="106"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24208_5#33" accession="ERX2663771">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663771</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24208_5#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24208_5#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495254W:A5, constructed from sample accession ERS1903934 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24208_5).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903934">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903934</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278956</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495254W:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#1" accession="ERX2663772">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663772</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D5, constructed from sample accession ERS1904147 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#4" accession="ERX2663773">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663773</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:G5, constructed from sample accession ERS1904150 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#7" accession="ERX2663774">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663774</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:B6, constructed from sample accession ERS1904153 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904153">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#18" accession="ERX2663775">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663775</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:E7, constructed from sample accession ERS1904164 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="383" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#21" accession="ERX2663776">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663776</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:H7, constructed from sample accession ERS1904167 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904167">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#24" accession="ERX2663777">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663777</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:C8, constructed from sample accession ERS1904170 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904170">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="91"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#27" accession="ERX2663778">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663778</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:F8, constructed from sample accession ERS1904173 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904173">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#30" accession="ERX2663779">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663779</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:A9, constructed from sample accession ERS1904176 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904176">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_1#33" accession="ERX2663780">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663780</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D9, constructed from sample accession ERS1904179 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_1).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904179">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="393" NOMINAL_SDEV="97"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#1" accession="ERX2663781">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663781</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D5, constructed from sample accession ERS1904147 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="379" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#4" accession="ERX2663782">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663782</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:G5, constructed from sample accession ERS1904150 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904150">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#15" accession="ERX2663783">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663783</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:B7, constructed from sample accession ERS1904161 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904161">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#18" accession="ERX2663784">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663784</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:E7, constructed from sample accession ERS1904164 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904164">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#21" accession="ERX2663785">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663785</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:H7, constructed from sample accession ERS1904167 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904167">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279189</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="368" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#24" accession="ERX2663786">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663786</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:C8, constructed from sample accession ERS1904170 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904170">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279192</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#27" accession="ERX2663787">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663787</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:F8, constructed from sample accession ERS1904173 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904173">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#30" accession="ERX2663788">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663788</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:A9, constructed from sample accession ERS1904176 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TTGTTCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904176">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279198</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_2#33" accession="ERX2663789">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663789</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D9, constructed from sample accession ERS1904179 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_2).  This submission includes reads tagged with the sequence TGCGTGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904179">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279201</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#1" accession="ERX2663790">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663790</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:A1, constructed from sample accession ERS1904322 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904322">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279344</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#12" accession="ERX2663791">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663791</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:D2, constructed from sample accession ERS1904333 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904333">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279355</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="420" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#15" accession="ERX2663792">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663792</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:G2, constructed from sample accession ERS1904336 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904336">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#18" accession="ERX2663793">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663793</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:B3, constructed from sample accession ERS1904339 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904339">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279361</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#21" accession="ERX2663794">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663794</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:F3, constructed from sample accession ERS1904343 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904343">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="381" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#24" accession="ERX2663795">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663795</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:B4, constructed from sample accession ERS1904347 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#27" accession="ERX2663796">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663796</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:E4, constructed from sample accession ERS1904350 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904350">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="421" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#30" accession="ERX2663797">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663797</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:H4, constructed from sample accession ERS1904353 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904353">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="104"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_3#33" accession="ERX2663798">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663798</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:C5, constructed from sample accession ERS1904356 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_3).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904356">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279378</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="389" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#11" accession="ERX2663799">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663799</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:C2, constructed from sample accession ERS1904332 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904332">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="415" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#14" accession="ERX2663800">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663800</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:F2, constructed from sample accession ERS1904335 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904335">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="404" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#17" accession="ERX2663801">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663801</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:A3, constructed from sample accession ERS1904338 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904338">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279360</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#20" accession="ERX2663802">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663802</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:E3, constructed from sample accession ERS1904342 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904342">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279364</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="405" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#23" accession="ERX2663803">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663803</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:A4, constructed from sample accession ERS1904346 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904346">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279368</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="413" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#26" accession="ERX2663804">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663804</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:D4, constructed from sample accession ERS1904349 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904349">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279371</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#29" accession="ERX2663805">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663805</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:G4, constructed from sample accession ERS1904352 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279374</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_4#32" accession="ERX2663806">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663806</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_4#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_4#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:B5, constructed from sample accession ERS1904355 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_4).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904355">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279377</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#10" accession="ERX2663807">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663807</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:B2, constructed from sample accession ERS1904331 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904331">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279353</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#13" accession="ERX2663808">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:E2, constructed from sample accession ERS1904334 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904334">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279356</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="410" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#16" accession="ERX2663809">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:H2, constructed from sample accession ERS1904337 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904337">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279359</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="427" NOMINAL_SDEV="98"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#19" accession="ERX2663810">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:D3, constructed from sample accession ERS1904341 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#22" accession="ERX2663811">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:G3, constructed from sample accession ERS1904344 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904344">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279366</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="411" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#25" accession="ERX2663812">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:C4, constructed from sample accession ERS1904348 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279370</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#28" accession="ERX2663813">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:F4, constructed from sample accession ERS1904351 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279373</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_5#31" accession="ERX2663814">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663814</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_5#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_5#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:A5, constructed from sample accession ERS1904354 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_5).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904354">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_6#1" accession="ERX2663815">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663815</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:D5, constructed from sample accession ERS1904357 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_6).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="327" NOMINAL_SDEV="100"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_6#9" accession="ERX2663816">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663816</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:D6, constructed from sample accession ERS1904365 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_6).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279387</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_6#12" accession="ERX2663817">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663817</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:G6, constructed from sample accession ERS1904368 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_6).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904368">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279390</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="318" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_6#15" accession="ERX2663818">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663818</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:B7, constructed from sample accession ERS1904371 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_6).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904371">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279393</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_6#18" accession="ERX2663819">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663819</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:E7, constructed from sample accession ERS1904374 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_6).  This submission includes reads tagged with the sequence TACCGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904374">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279396</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_6#21" accession="ERX2663820">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663820</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:H7, constructed from sample accession ERS1904377 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_6).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="334" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_6#24" accession="ERX2663821">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663821</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:C8, constructed from sample accession ERS1904380 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_6).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_7#2" accession="ERX2663822">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663822</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:E5, constructed from sample accession ERS1904358 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_7).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279380</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="392" NOMINAL_SDEV="93"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_7#5" accession="ERX2663823">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663823</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:H5, constructed from sample accession ERS1904361 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_7).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904361">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279383</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_7#8" accession="ERX2663824">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663824</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:C6, constructed from sample accession ERS1904364 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_7).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279386</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="351" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_7#16" accession="ERX2663825">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663825</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:C7, constructed from sample accession ERS1904372 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_7).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279394</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_7#19" accession="ERX2663826">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663826</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:F7, constructed from sample accession ERS1904375 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_7).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904375">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279397</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="371" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_7#22" accession="ERX2663827">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663827</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:A8, constructed from sample accession ERS1904378 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_7).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904378">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279400</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24209_7#25" accession="ERX2663828">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663828</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24209_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24209_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:D8, constructed from sample accession ERS1904381 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24209_7).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="355" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_1#3" accession="ERX2663829">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663829</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A6, constructed from sample accession ERS1887990 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_1).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887990">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887990</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="238" NOMINAL_SDEV="162"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_1#6" accession="ERX2663830">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663830</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B6, constructed from sample accession ERS1887991 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_1).  This submission includes reads tagged with the sequence ACACAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887991">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887991</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="430" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_1#9" accession="ERX2663831">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663831</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C6, constructed from sample accession ERS1887993 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_1).  This submission includes reads tagged with the sequence CAACCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887993">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887993</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_1#12" accession="ERX2663832">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663832</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D6, constructed from sample accession ERS1887994 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_1).  This submission includes reads tagged with the sequence CGCATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887994">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887994</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="234"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_1#15" accession="ERX2663833">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663833</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E6, constructed from sample accession ERS1887995 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_1).  This submission includes reads tagged with the sequence GGAGAACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887995">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887995</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="419" NOMINAL_SDEV="217"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_1#23" accession="ERX2663834">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663834</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H5, constructed from sample accession ERS1887989 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_1).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="405" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#2" accession="ERX2663835">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663835</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A5, constructed from sample accession ERS1887982 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887982">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887982</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#5" accession="ERX2663836">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663836</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B5, constructed from sample accession ERS1887983 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence AAGGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887983">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887983</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#8" accession="ERX2663837">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663837</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C5, constructed from sample accession ERS1887984 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence ATTGAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887984">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887984</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="491" NOMINAL_SDEV="109"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#11" accession="ERX2663838">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663838</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D5, constructed from sample accession ERS1887985 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence CGACTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887985">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887985</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="402" NOMINAL_SDEV="198"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#14" accession="ERX2663839">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663839</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E5, constructed from sample accession ERS1887986 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887986">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887986</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="489" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#17" accession="ERX2663840">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663840</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F5, constructed from sample accession ERS1887987 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887987">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887987</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="196" NOMINAL_SDEV="24"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#20" accession="ERX2663841">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663841</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G5, constructed from sample accession ERS1887988 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887988">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887988</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="424" NOMINAL_SDEV="230"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_2#23" accession="ERX2663842">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663842</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H5, constructed from sample accession ERS1887989 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_2).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887989">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887989</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="125"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_3#7" accession="ERX2663843">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663843</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C7, constructed from sample accession ERS1888001 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_3).  This submission includes reads tagged with the sequence GACTAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888001">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888001</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="456" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_3#10" accession="ERX2663844">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663844</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D7, constructed from sample accession ERS1888002 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_3).  This submission includes reads tagged with the sequence CTCAATGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888002">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888002</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="355" NOMINAL_SDEV="126"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_3#13" accession="ERX2663845">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663845</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E7, constructed from sample accession ERS1888003 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_3).  This submission includes reads tagged with the sequence GGTGCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888003">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888003</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="446" NOMINAL_SDEV="225"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_3#16" accession="ERX2663846">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663846</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F7, constructed from sample accession ERS1888004 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_3).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888004">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888004</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="216"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_3#19" accession="ERX2663847">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663847</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G7, constructed from sample accession ERS1888005 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_3).  This submission includes reads tagged with the sequence AGGCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888005">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="184" NOMINAL_SDEV="32"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_3#22" accession="ERX2663848">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663848</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H7, constructed from sample accession ERS1888006 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_3).  This submission includes reads tagged with the sequence CTAAGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_4#2" accession="ERX2663849">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663849</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A8, constructed from sample accession ERS1888008 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_4).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="185"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_4#5" accession="ERX2663850">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663850</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B8, constructed from sample accession ERS1888027 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_4).  This submission includes reads tagged with the sequence ACCTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="409" NOMINAL_SDEV="187"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_4#8" accession="ERX2663851">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663851</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C8, constructed from sample accession ERS1888029 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_4).  This submission includes reads tagged with the sequence CAATGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299" NOMINAL_SDEV="223"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_4#16" accession="ERX2663852">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663852</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F7, constructed from sample accession ERS1888004 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_4).  This submission includes reads tagged with the sequence TGGTGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888004">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888004</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="223"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_4#19" accession="ERX2663853">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663853</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G7, constructed from sample accession ERS1888005 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_4).  This submission includes reads tagged with the sequence AGGCTAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888005">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888005</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="164" NOMINAL_SDEV="160"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_4#22" accession="ERX2663854">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663854</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H7, constructed from sample accession ERS1888006 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_4).  This submission includes reads tagged with the sequence CTAAGGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888006">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888006</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_5#2" accession="ERX2663855">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663855</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A8, constructed from sample accession ERS1888008 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_5).  This submission includes reads tagged with the sequence CATCAAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888008">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888008</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="396" NOMINAL_SDEV="221"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_5#5" accession="ERX2663856">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663856</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B8, constructed from sample accession ERS1888027 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_5).  This submission includes reads tagged with the sequence ACCTCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888027">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888027</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229009</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="349" NOMINAL_SDEV="205"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_5#8" accession="ERX2663857">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663857</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C8, constructed from sample accession ERS1888029 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_5).  This submission includes reads tagged with the sequence CAATGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888029">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888029</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229011</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="284" NOMINAL_SDEV="194"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_5#11" accession="ERX2663858">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663858</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D8, constructed from sample accession ERS1888032 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_5).  This submission includes reads tagged with the sequence CTGAGCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888032">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888032</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229014</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="434" NOMINAL_SDEV="73"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_5#14" accession="ERX2663859">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663859</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_5#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_5#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E8, constructed from sample accession ERS1888014 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_5).  This submission includes reads tagged with the sequence GTACGCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888014">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888014</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="155" NOMINAL_SDEV="7"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_5#17" accession="ERX2663860">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663860</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_5#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_5#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F8, constructed from sample accession ERS1888016 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_5).  This submission includes reads tagged with the sequence TTCACGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888016">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888016</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="204" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#2" accession="ERX2663861">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663861</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A11, constructed from sample accession ERS1888063 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence CTGTAGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888063">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888063</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229045</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="492" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#5" accession="ERX2663862">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663862</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B11, constructed from sample accession ERS1888064 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence ACTATGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888064">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888064</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229046</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="181" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#8" accession="ERX2663863">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663863</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C11, constructed from sample accession ERS1888065 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence CATACCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888065">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888065</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229047</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="182" NOMINAL_SDEV="23"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#11" accession="ERX2663864">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663864</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D11, constructed from sample accession ERS1888066 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence CAAGACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888066">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888066</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229048</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="230"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#14" accession="ERX2663865">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663865</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E11, constructed from sample accession ERS1888067 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence GTGTTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888067">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888067</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229049</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="187" NOMINAL_SDEV="46"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#17" accession="ERX2663866">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663866</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F11, constructed from sample accession ERS1888068 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence AAGGACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888068">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888068</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229050</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="333" NOMINAL_SDEV="155"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#20" accession="ERX2663867">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663867</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G11, constructed from sample accession ERS1888070 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence CAAGGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888070">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888070</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229052</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="190" NOMINAL_SDEV="76"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_6#23" accession="ERX2663868">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663868</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H10, constructed from sample accession ERS1888062 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_6).  This submission includes reads tagged with the sequence GAGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888062">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888062</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229044</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="197" NOMINAL_SDEV="57"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_7#10" accession="ERX2663869">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663869</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D10, constructed from sample accession ERS1888058 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_7).  This submission includes reads tagged with the sequence GAATCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888058">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888058</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229040</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="208" NOMINAL_SDEV="41"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_7#13" accession="ERX2663870">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663870</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E10, constructed from sample accession ERS1888059 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_7).  This submission includes reads tagged with the sequence GTCTGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888059">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888059</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229041</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="433" NOMINAL_SDEV="129"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_7#16" accession="ERX2663871">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663871</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F10, constructed from sample accession ERS1888060 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_7).  This submission includes reads tagged with the sequence AAGAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888060">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888060</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229042</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="275" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_7#19" accession="ERX2663872">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663872</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G10, constructed from sample accession ERS1888061 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_7).  This submission includes reads tagged with the sequence ATTGGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888061">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888061</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229043</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="291" NOMINAL_SDEV="219"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_7#22" accession="ERX2663873">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663873</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H9, constructed from sample accession ERS1888052 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_7).  This submission includes reads tagged with the sequence GACAGTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888052">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888052</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="165" NOMINAL_SDEV="15"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_8#1" accession="ERX2663874">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663874</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A10, constructed from sample accession ERS1888053 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_8).  This submission includes reads tagged with the sequence ACAAGCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888053">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888053</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="141"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_8#4" accession="ERX2663875">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663875</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B10, constructed from sample accession ERS1888056 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_8).  This submission includes reads tagged with the sequence ACGTATCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888056">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888056</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229038</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="195" NOMINAL_SDEV="5"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_8#7" accession="ERX2663876">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663876</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C10, constructed from sample accession ERS1888057 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_8).  This submission includes reads tagged with the sequence CAGCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888057">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888057</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229039</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_8#18" accession="ERX2663877">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663877</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F12, constructed from sample accession ERS1888077 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_8).  This submission includes reads tagged with the sequence AATCCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888077">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888077</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="187" NOMINAL_SDEV="13"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_8#21" accession="ERX2663878">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663878</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G12, constructed from sample accession ERS1888079 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_8).  This submission includes reads tagged with the sequence CACCTTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888079">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888079</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="193" NOMINAL_SDEV="69"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24210_8#24" accession="ERX2663879">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663879</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24210_8#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24210_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H11, constructed from sample accession ERS1888071 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24210_8).  This submission includes reads tagged with the sequence GATGAATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888071">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888071</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229053</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="197" NOMINAL_SDEV="173"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#3" accession="ERX2663880">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663880</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F5, constructed from sample accession ERS1903729 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903729">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903729</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#6" accession="ERX2663881">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663881</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:A6, constructed from sample accession ERS1903732 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903732">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903732</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#9" accession="ERX2663882">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663882</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:D6, constructed from sample accession ERS1903735 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903735">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903735</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:D6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="407" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#12" accession="ERX2663883">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663883</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:G6, constructed from sample accession ERS1903738 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903738">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903738</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:G6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#15" accession="ERX2663884">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663884</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:B7, constructed from sample accession ERS1903741 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903741">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903741</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="378" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#26" accession="ERX2663885">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663885</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:E8, constructed from sample accession ERS1903752 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TGCTGATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903752">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903752</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:E8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="397" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#29" accession="ERX2663886">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663886</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:H8, constructed from sample accession ERS1903755 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TCTCTTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903755">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903755</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:H8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="380" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#32" accession="ERX2663887">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663887</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:C9, constructed from sample accession ERS1903758 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence TACCACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903758">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903758</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:C9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="372" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_1#35" accession="ERX2663888">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663888</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495251T:F9, constructed from sample accession ERS1903761 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_1).  This submission includes reads tagged with the sequence GATCTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1903761">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1903761</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104278783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495251T:F9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="84"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#3" accession="ERX2663889">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663889</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:C1, constructed from sample accession ERS1904114 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904114">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904114</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#6" accession="ERX2663890">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663890</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:F1, constructed from sample accession ERS1904117 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904117">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904117</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="362" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#9" accession="ERX2663891">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663891</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:A2, constructed from sample accession ERS1904120 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904120">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904120</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="395" NOMINAL_SDEV="90"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#12" accession="ERX2663892">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663892</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D2, constructed from sample accession ERS1904123 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904123">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904123</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="361" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#23" accession="ERX2663893">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663893</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:H3, constructed from sample accession ERS1904135 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904135">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="355" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#26" accession="ERX2663894">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663894</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:C4, constructed from sample accession ERS1904138 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904138">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="403" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#29" accession="ERX2663895">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663895</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:F4, constructed from sample accession ERS1904141 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904141">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="391" NOMINAL_SDEV="94"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_2#32" accession="ERX2663896">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663896</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:A5, constructed from sample accession ERS1904144 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_2).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904144">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="89"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#1" accession="ERX2663897">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663897</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:A1, constructed from sample accession ERS1904112 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904112">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904112</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="360" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#4" accession="ERX2663898">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663898</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D1, constructed from sample accession ERS1904115 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904115">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904115</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#7" accession="ERX2663899">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663899</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:G1, constructed from sample accession ERS1904118 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904118">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904118</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="360" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#10" accession="ERX2663900">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663900</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:B2, constructed from sample accession ERS1904121 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904121">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904121</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="375" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#21" accession="ERX2663901">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663901</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:E3, constructed from sample accession ERS1904132 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#24" accession="ERX2663902">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663902</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:A4, constructed from sample accession ERS1904136 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904136">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#27" accession="ERX2663903">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663903</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:D4, constructed from sample accession ERS1904139 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904139">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="366" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#30" accession="ERX2663904">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663904</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:G4, constructed from sample accession ERS1904142 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904142">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_3#33" accession="ERX2663905">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663905</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:B5, constructed from sample accession ERS1904145 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_3).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904145">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="384" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#2" accession="ERX2663906">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663906</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:B1, constructed from sample accession ERS1904113 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904113">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904113</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="355" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#5" accession="ERX2663907">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663907</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:E1, constructed from sample accession ERS1904116 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904116">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904116</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="357" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#8" accession="ERX2663908">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663908</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:H1, constructed from sample accession ERS1904119 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904119">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904119</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="377" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#19" accession="ERX2663909">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663909</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:C3, constructed from sample accession ERS1904130 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904130">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904130</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="355" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#22" accession="ERX2663910">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663910</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:G3, constructed from sample accession ERS1904134 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904134">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="353" NOMINAL_SDEV="79"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#25" accession="ERX2663911">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663911</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:B4, constructed from sample accession ERS1904137 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904137">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="358" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#28" accession="ERX2663912">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663912</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:E4, constructed from sample accession ERS1904140 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904140">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="374" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#31" accession="ERX2663913">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663913</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:H4, constructed from sample accession ERS1904143 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904143">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="367" NOMINAL_SDEV="88"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24248_4#34" accession="ERX2663914">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663914</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24248_4#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24248_4#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495269G:C5, constructed from sample accession ERS1904146 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24248_4).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904146">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495269G:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_1#3" accession="ERX2663915">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663915</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:A6, constructed from sample accession ERS1888472 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_1).  This submission includes reads tagged with the sequence ACATTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888472">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888472</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:A6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="166" NOMINAL_SDEV="14"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_1#6" accession="ERX2663916">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663916</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:B5, constructed from sample accession ERS1888450 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_1).  This submission includes reads tagged with the sequence AAGGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888450">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="294" NOMINAL_SDEV="83"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_1#9" accession="ERX2663917">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663917</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:C4, constructed from sample accession ERS1888432 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_1).  This submission includes reads tagged with the sequence ATCCTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888432">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229414</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:C4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="166" NOMINAL_SDEV="9"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_1#17" accession="ERX2663918">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663918</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:E5, constructed from sample accession ERS1888456 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_1).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="236" NOMINAL_SDEV="69"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_1#20" accession="ERX2663919">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663919</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:F5, constructed from sample accession ERS1888457 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_1).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888457">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="202" NOMINAL_SDEV="113"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_1#23" accession="ERX2663920">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663920</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:G5, constructed from sample accession ERS1888458 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_1).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888458">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="184" NOMINAL_SDEV="152"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_1#25" accession="ERX2663921">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663921</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:H4, constructed from sample accession ERS1888441 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_1).  This submission includes reads tagged with the sequence CCTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888441">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="24"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_2#2" accession="ERX2663922">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663922</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:A5, constructed from sample accession ERS1888444 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_2).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888444">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_2#5" accession="ERX2663923">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663923</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:B4, constructed from sample accession ERS1888431 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_2).  This submission includes reads tagged with the sequence AAGACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888431">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229413</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:B4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="198" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_2#8" accession="ERX2663924">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663924</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:B7, constructed from sample accession ERS1888509 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_2).  This submission includes reads tagged with the sequence ACAGCAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888509">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888509</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229491</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:B7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="173" NOMINAL_SDEV="2"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_2#11" accession="ERX2663925">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663925</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:C6, constructed from sample accession ERS1888474 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_2).  This submission includes reads tagged with the sequence CAACCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888474">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888474</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:C6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="193" NOMINAL_SDEV="21"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_2#14" accession="ERX2663926">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663926</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:D5, constructed from sample accession ERS1888455 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_2).  This submission includes reads tagged with the sequence CGACTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888455">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="359" NOMINAL_SDEV="138"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_2#17" accession="ERX2663927">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663927</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:E5, constructed from sample accession ERS1888456 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_2).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888456">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="224" NOMINAL_SDEV="63"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#1" accession="ERX2663928">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663928</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:A4, constructed from sample accession ERS1888427 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence AGTGGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888427">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229409</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:A4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="258" NOMINAL_SDEV="64"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#4" accession="ERX2663929">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663929</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:A7, constructed from sample accession ERS1888501 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888501">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888501</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:A7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#7" accession="ERX2663930">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663930</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:B6, constructed from sample accession ERS1888473 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence ACACAGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888473">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888473</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="418"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#10" accession="ERX2663931">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663931</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:C5, constructed from sample accession ERS1888454 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence ATTGAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888454">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="360" NOMINAL_SDEV="173"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#13" accession="ERX2663932">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663932</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:D4, constructed from sample accession ERS1888433 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence CGAACTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888433">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229415</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="159" NOMINAL_SDEV="162"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#16" accession="ERX2663933">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663933</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:E4, constructed from sample accession ERS1888434 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence GCTAACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888434">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229416</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="184" NOMINAL_SDEV="11"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#19" accession="ERX2663934">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663934</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:F4, constructed from sample accession ERS1888435 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888435">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229417</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="354" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_3#22" accession="ERX2663935">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663935</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:G4, constructed from sample accession ERS1888437 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_3).  This submission includes reads tagged with the sequence AGATGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888437">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="168" NOMINAL_SDEV="11"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_4#2" accession="ERX2663936">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663936</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:A2, constructed from sample accession ERS1888348 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_4).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="213" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_4#10" accession="ERX2663937">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663937</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:D2, constructed from sample accession ERS1888358 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_4).  This submission includes reads tagged with the sequence CCGTGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888358">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229340</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_4#13" accession="ERX2663938">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663938</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:E2, constructed from sample accession ERS1888364 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_4).  This submission includes reads tagged with the sequence GCCACATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888364">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229346</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_4#16" accession="ERX2663939">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663939</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:F2, constructed from sample accession ERS1888365 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_4).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888365">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229347</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_4#19" accession="ERX2663940">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663940</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:G2, constructed from sample accession ERS1888370 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_4).  This submission includes reads tagged with the sequence ACACGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322" NOMINAL_SDEV="177"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_4#22" accession="ERX2663941">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663941</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:H2, constructed from sample accession ERS1888372 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_4).  This submission includes reads tagged with the sequence CCGACAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="334" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_5#2" accession="ERX2663942">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663942</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:A2, constructed from sample accession ERS1888348 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_5).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="216" NOMINAL_SDEV="55"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_5#5" accession="ERX2663943">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663943</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:B2, constructed from sample accession ERS1888352 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_5).  This submission includes reads tagged with the sequence AACCGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="318"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_5#8" accession="ERX2663944">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663944</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:C3, constructed from sample accession ERS1888380 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_5).  This submission includes reads tagged with the sequence AGTCACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="248" NOMINAL_SDEV="8"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_5#11" accession="ERX2663945">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663945</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:D3, constructed from sample accession ERS1888383 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_5).  This submission includes reads tagged with the sequence CCTCCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="359" NOMINAL_SDEV="99"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_5#19" accession="ERX2663946">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663946</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:G2, constructed from sample accession ERS1888370 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_5).  This submission includes reads tagged with the sequence ACACGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888370">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229352</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="303" NOMINAL_SDEV="162"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_5#22" accession="ERX2663947">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663947</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:H2, constructed from sample accession ERS1888372 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_5).  This submission includes reads tagged with the sequence CCGACAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888372">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229354</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:H2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="335" NOMINAL_SDEV="85"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_6#2" accession="ERX2663948">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663948</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:A2, constructed from sample accession ERS1888348 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_6).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888348">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229330</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="211" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_6#5" accession="ERX2663949">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663949</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:B2, constructed from sample accession ERS1888352 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_6).  This submission includes reads tagged with the sequence AACCGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888352">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229334</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_6#8" accession="ERX2663950">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663950</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:C3, constructed from sample accession ERS1888380 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_6).  This submission includes reads tagged with the sequence AGTCACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229362</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="246" NOMINAL_SDEV="5"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_6#11" accession="ERX2663951">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663951</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:D3, constructed from sample accession ERS1888383 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_6).  This submission includes reads tagged with the sequence CCTCCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888383">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229365</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:D3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="364" NOMINAL_SDEV="135"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_6#14" accession="ERX2663952">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663952</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_6#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_6#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:E3, constructed from sample accession ERS1888390 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_6).  This submission includes reads tagged with the sequence GCGAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888390">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229372</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_6#17" accession="ERX2663953">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663953</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_6#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_6#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:F3, constructed from sample accession ERS1888393 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_6).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888393">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229375</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_6#20" accession="ERX2663954">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663954</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499666I:G3, constructed from sample accession ERS1888394 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_6).  This submission includes reads tagged with the sequence ACAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888394">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229376</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499666I:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="408" NOMINAL_SDEV="39"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_7#5" accession="ERX2663955">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663955</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:B5, constructed from sample accession ERS1888243 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_7).  This submission includes reads tagged with the sequence AAGGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="390"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_7#8" accession="ERX2663956">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663956</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:C5, constructed from sample accession ERS1888245 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_7).  This submission includes reads tagged with the sequence ATTGAGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888245">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888245</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229227</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:C5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="206" NOMINAL_SDEV="56"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_7#11" accession="ERX2663957">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663957</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:D5, constructed from sample accession ERS1888248 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_7).  This submission includes reads tagged with the sequence CGACTGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888248">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888248</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229230</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="394" NOMINAL_SDEV="152"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_7#14" accession="ERX2663958">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663958</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:E5, constructed from sample accession ERS1888251 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_7).  This submission includes reads tagged with the sequence GCTCGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888251">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229233</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:E5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="255" NOMINAL_SDEV="231"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_7#17" accession="ERX2663959">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663959</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:F5, constructed from sample accession ERS1888252 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_7).  This submission includes reads tagged with the sequence TGGAACAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888252">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229234</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:F5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="243" NOMINAL_SDEV="77"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_7#20" accession="ERX2663960">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663960</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:G5, constructed from sample accession ERS1888257 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_7).  This submission includes reads tagged with the sequence AGCACCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888257">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229239</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="416" NOMINAL_SDEV="163"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_7#23" accession="ERX2663961">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663961</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:H5, constructed from sample accession ERS1888258 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_7).  This submission includes reads tagged with the sequence CGACACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888258">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229240</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_8#2" accession="ERX2663962">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663962</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:A5, constructed from sample accession ERS1888242 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_8).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888242">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_8#5" accession="ERX2663963">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663963</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:B5, constructed from sample accession ERS1888243 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_8).  This submission includes reads tagged with the sequence AAGGTACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229225</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:B5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="477"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_8#13" accession="ERX2663964">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663964</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:E4, constructed from sample accession ERS1888228 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_8).  This submission includes reads tagged with the sequence GCTAACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="376" NOMINAL_SDEV="150"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_8#16" accession="ERX2663965">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663965</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:F4, constructed from sample accession ERS1888229 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_8).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="237" NOMINAL_SDEV="120"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_8#19" accession="ERX2663966">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663966</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:G4, constructed from sample accession ERS1888236 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_8).  This submission includes reads tagged with the sequence AGATGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="197" NOMINAL_SDEV="139"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24294_8#22" accession="ERX2663967">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663967</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24294_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24294_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:H4, constructed from sample accession ERS1888241 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24294_8).  This submission includes reads tagged with the sequence CCTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_5#1" accession="ERX2663968">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663968</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:A1, constructed from sample accession ERS1887943 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_5).  This submission includes reads tagged with the sequence AACGTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887943">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887943</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="232" NOMINAL_SDEV="147"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_5#4" accession="ERX2663969">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663969</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:B1, constructed from sample accession ERS1887954 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_5).  This submission includes reads tagged with the sequence AACAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887954">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887954</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="412" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_5#7" accession="ERX2663970">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663970</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:C1, constructed from sample accession ERS1887958 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_5).  This submission includes reads tagged with the sequence AGATCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887958">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887958</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450" NOMINAL_SDEV="102"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_5#10" accession="ERX2663971">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663971</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:D1, constructed from sample accession ERS1887961 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_5).  This submission includes reads tagged with the sequence CCGAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887961">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887961</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="325" NOMINAL_SDEV="95"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_5#13" accession="ERX2663972">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663972</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:E1, constructed from sample accession ERS1887963 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_5).  This submission includes reads tagged with the sequence GATAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887963">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887963</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228945</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="185" NOMINAL_SDEV="7"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_5#21" accession="ERX2663973">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663973</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:G3, constructed from sample accession ERS1888189 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_5).  This submission includes reads tagged with the sequence ACAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888189">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888189</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:G3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_5#24" accession="ERX2663974">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663974</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:H3, constructed from sample accession ERS1888213 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_5).  This submission includes reads tagged with the sequence CCTAATCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888213">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888213</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229195</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="18"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_6#3" accession="ERX2663975">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663975</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:A3, constructed from sample accession ERS1888147 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_6).  This submission includes reads tagged with the sequence ATGCCTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888147">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:A3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="406" NOMINAL_SDEV="36"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_6#6" accession="ERX2663976">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663976</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:B3, constructed from sample accession ERS1888154 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_6).  This submission includes reads tagged with the sequence AACGCTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888154">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="190" NOMINAL_SDEV="38"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_6#9" accession="ERX2663977">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663977</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:C3, constructed from sample accession ERS1888167 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_6).  This submission includes reads tagged with the sequence AGTCACTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888167">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:C3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="175" NOMINAL_SDEV="7"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_6#12" accession="ERX2663978">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663978</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:D3, constructed from sample accession ERS1888178 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_6).  This submission includes reads tagged with the sequence CCTCCTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888178">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_6#15" accession="ERX2663979">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663979</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:E3, constructed from sample accession ERS1888180 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_6).  This submission includes reads tagged with the sequence GCGAGTAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888180">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888180</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="160"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_6#18" accession="ERX2663980">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663980</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:F3, constructed from sample accession ERS1888181 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_6).  This submission includes reads tagged with the sequence TCTTCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888181">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888181</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:F3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="186"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_7#5" accession="ERX2663981">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663981</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:B2, constructed from sample accession ERS1888007 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_7).  This submission includes reads tagged with the sequence AACCGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888007">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888007</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="171" NOMINAL_SDEV="167"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_7#8" accession="ERX2663982">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663982</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:C2, constructed from sample accession ERS1888042 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_7).  This submission includes reads tagged with the sequence AGCAGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888042">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888042</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229024</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="287" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_7#11" accession="ERX2663983">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663983</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:D2, constructed from sample accession ERS1888054 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_7).  This submission includes reads tagged with the sequence CCGTGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888054">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888054</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="439" NOMINAL_SDEV="48"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_7#14" accession="ERX2663984">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663984</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:E2, constructed from sample accession ERS1888055 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_7).  This submission includes reads tagged with the sequence GCCACATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888055">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888055</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="176" NOMINAL_SDEV="10"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_7#17" accession="ERX2663985">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663985</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:F2, constructed from sample accession ERS1888088 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_7).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888088">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888088</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_7#20" accession="ERX2663986">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663986</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:G2, constructed from sample accession ERS1888131 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_7).  This submission includes reads tagged with the sequence ACACGACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888131">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888131</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="228" NOMINAL_SDEV="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_7#23" accession="ERX2663987">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663987</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:H2, constructed from sample accession ERS1888146 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_7).  This submission includes reads tagged with the sequence CCGACAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888146">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_8#2" accession="ERX2663988">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663988</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:A5, constructed from sample accession ERS1888242 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_8).  This submission includes reads tagged with the sequence ACCACTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888242">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888242</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229224</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="226"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_8#13" accession="ERX2663989">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663989</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:E4, constructed from sample accession ERS1888228 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_8).  This submission includes reads tagged with the sequence GCTAACGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888228">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888228</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229210</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:E4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="363" NOMINAL_SDEV="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_8#16" accession="ERX2663990">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663990</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:F4, constructed from sample accession ERS1888229 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_8).  This submission includes reads tagged with the sequence TGAAGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888229">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888229</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229211</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="195" NOMINAL_SDEV="96"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_8#19" accession="ERX2663991">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663991</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:G4, constructed from sample accession ERS1888236 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_8).  This submission includes reads tagged with the sequence AGATGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888236">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888236</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229218</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:G4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="197" NOMINAL_SDEV="134"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24297_8#22" accession="ERX2663992">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663992</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24297_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24297_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN499665H:H4, constructed from sample accession ERS1888241 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24297_8).  This submission includes reads tagged with the sequence CCTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888241">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888241</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229223</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN499665H:H4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24420_8#1" accession="ERX2663993">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663993</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24420_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24420_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:D5, constructed from sample accession ERS1904357 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24420_8).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904357">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279379</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="369" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24420_8#4" accession="ERX2663994">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24420_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24420_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:G5, constructed from sample accession ERS1904360 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24420_8).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904360">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279382</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="354" NOMINAL_SDEV="80"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24420_8#7" accession="ERX2663995">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24420_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24420_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:B6, constructed from sample accession ERS1904363 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24420_8).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279385</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="350" NOMINAL_SDEV="82"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24420_8#10" accession="ERX2663996">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663996</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24420_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24420_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:E6, constructed from sample accession ERS1904366 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24420_8).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904366">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279388</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:E6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="399" NOMINAL_SDEV="92"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24420_8#21" accession="ERX2663997">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663997</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24420_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24420_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:H7, constructed from sample accession ERS1904377 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24420_8).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904377">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279399</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:H7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="334" NOMINAL_SDEV="81"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24420_8#24" accession="ERX2663998">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663998</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24420_8#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24420_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495272B:C8, constructed from sample accession ERS1904380 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24420_8).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1904380">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1904380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104279402</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495272B:C8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="387" NOMINAL_SDEV="87"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_7#2" accession="ERX2663999">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2663999</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:A2, constructed from sample accession ERS1887949 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_7).  This submission includes reads tagged with the sequence AAACATCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887949">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887949</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:A2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="159" NOMINAL_SDEV="216"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_7#5" accession="ERX2664000">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664000</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B2, constructed from sample accession ERS1887950 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_7).  This submission includes reads tagged with the sequence AACCGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887950">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887950</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="492" NOMINAL_SDEV="196"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_7#8" accession="ERX2664001">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664001</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C2, constructed from sample accession ERS1887951 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_7).  This submission includes reads tagged with the sequence AGCAGGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887951">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887951</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302" NOMINAL_SDEV="151"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_7#11" accession="ERX2664002">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664002</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D2, constructed from sample accession ERS1887952 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_7).  This submission includes reads tagged with the sequence CCGTGAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887952">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887952</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="447" NOMINAL_SDEV="123"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_7#14" accession="ERX2664003">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664003</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E2, constructed from sample accession ERS1887953 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_7).  This submission includes reads tagged with the sequence GCCACATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887953">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887953</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="443" NOMINAL_SDEV="111"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_7#17" accession="ERX2664004">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664004</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F2, constructed from sample accession ERS1887956 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_7).  This submission includes reads tagged with the sequence TCCGTCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887956">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887956</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="453" NOMINAL_SDEV="145"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_8#4" accession="ERX2664005">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664005</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:B1, constructed from sample accession ERS1887941 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_8).  This submission includes reads tagged with the sequence AACAACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887941">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887941</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:B1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="214" NOMINAL_SDEV="235"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_8#7" accession="ERX2664006">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664006</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:C1, constructed from sample accession ERS1887942 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_8).  This submission includes reads tagged with the sequence AGATCGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887942">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887942</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:C1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="515" NOMINAL_SDEV="117"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_8#10" accession="ERX2664007">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664007</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:D1, constructed from sample accession ERS1887944 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_8).  This submission includes reads tagged with the sequence CCGAAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887944">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887944</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="437" NOMINAL_SDEV="239"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_8#13" accession="ERX2664008">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664008</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:E1, constructed from sample accession ERS1887945 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_8).  This submission includes reads tagged with the sequence GATAGACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887945">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887945</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:E1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="460" NOMINAL_SDEV="128"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_8#16" accession="ERX2664009">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664009</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:F1, constructed from sample accession ERS1887946 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_8).  This submission includes reads tagged with the sequence TATCAGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887946">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887946</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:F1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="457" NOMINAL_SDEV="176"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_8#19" accession="ERX2664010">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664010</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:G1, constructed from sample accession ERS1887947 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_8).  This submission includes reads tagged with the sequence AATGTTGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887947">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887947</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="194" NOMINAL_SDEV="44"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_24433_8#22" accession="ERX2664011">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664011</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_24433_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_24433_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN495716I:H1, constructed from sample accession ERS1887948 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (24433_8).  This submission includes reads tagged with the sequence CCATCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887948">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887948</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN495716I:H1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="227" NOMINAL_SDEV="158"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#2" accession="ERX2664012">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664012</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:F7, constructed from sample accession ERS1888347 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence CAACCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#5" accession="ERX2664013">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664013</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A8, constructed from sample accession ERS1888351 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence GATGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#8" accession="ERX2664014">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D8, constructed from sample accession ERS1888367 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence CGCGCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#11" accession="ERX2664015">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664015</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G8, constructed from sample accession ERS1888387 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence CAGGTTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888387">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229369</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="229" NOMINAL_SDEV="74"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#14" accession="ERX2664016">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B9, constructed from sample accession ERS1888436 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence GAAGAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888436">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229418</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="157"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#17" accession="ERX2664017">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E9, constructed from sample accession ERS1888502 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence AAGAGAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888502">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888502</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:E9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="382" NOMINAL_SDEV="53"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#20" accession="ERX2664018">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H9, constructed from sample accession ERS1888505 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence CATTGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888505">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888505</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:H9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="257" NOMINAL_SDEV="86"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#23" accession="ERX2664019">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:C10, constructed from sample accession ERS1888508 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence CTCACGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888508">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888508</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229490</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:C10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="344" NOMINAL_SDEV="156"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_1#26" accession="ERX2664020">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:F10, constructed from sample accession ERS1888513 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_1).  This submission includes reads tagged with the sequence TGTGTGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888513">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888513</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229495</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_2#7" accession="ERX2664021">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:C8, constructed from sample accession ERS1888363 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_2).  This submission includes reads tagged with the sequence TCGGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888363">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229345</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_2#10" accession="ERX2664022">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664022</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:F8, constructed from sample accession ERS1888381 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_2).  This submission includes reads tagged with the sequence TGGTGCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888381">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229363</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:F8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="174"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_2#13" accession="ERX2664023">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664023</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A9, constructed from sample accession ERS1888421 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_2).  This submission includes reads tagged with the sequence CTACGGCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888421">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229403</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:A9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_2#16" accession="ERX2664024">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664024</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D9, constructed from sample accession ERS1888445 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_2).  This submission includes reads tagged with the sequence CGAACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="153"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_2#19" accession="ERX2664025">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G9, constructed from sample accession ERS1888504 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_2).  This submission includes reads tagged with the sequence TGAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888504">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888504</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="239" NOMINAL_SDEV="120"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_2#22" accession="ERX2664026">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B10, constructed from sample accession ERS1888507 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_2).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888507">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888507</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25154_2#25" accession="ERX2664027">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25154_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25154_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E10, constructed from sample accession ERS1888512 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25154_2).  This submission includes reads tagged with the sequence TCAACGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="343" NOMINAL_SDEV="205"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_1#1" accession="ERX2664028">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A1, constructed from sample accession ERS1887968 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_1).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="287" NOMINAL_SDEV="153"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_1#4" accession="ERX2664029">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D1, constructed from sample accession ERS1888069 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_1).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888069">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="226" NOMINAL_SDEV="52"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_1#12" accession="ERX2664030">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D2, constructed from sample accession ERS1888184 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_1).  This submission includes reads tagged with the sequence GTCGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888184">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_1#15" accession="ERX2664031">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G2, constructed from sample accession ERS1888208 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_1).  This submission includes reads tagged with the sequence GTACAGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888208">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888208</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229190</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="400" NOMINAL_SDEV="68"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_1#18" accession="ERX2664032">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B3, constructed from sample accession ERS1888215 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_1).  This submission includes reads tagged with the sequence CTGGCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888215">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888215</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="192"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_1#21" accession="ERX2664033">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E3, constructed from sample accession ERS1888220 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_1).  This submission includes reads tagged with the sequence CGCTATTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="194" NOMINAL_SDEV="49"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_1#24" accession="ERX2664034">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H3, constructed from sample accession ERS1888231 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_1).  This submission includes reads tagged with the sequence TTCGAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="124"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_2#1" accession="ERX2664035">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A1, constructed from sample accession ERS1887968 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_2).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="385" NOMINAL_SDEV="142"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_2#4" accession="ERX2664036">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D1, constructed from sample accession ERS1888069 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_2).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888069">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="274" NOMINAL_SDEV="107"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_2#7" accession="ERX2664037">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G1, constructed from sample accession ERS1888132 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_2).  This submission includes reads tagged with the sequence AAGTTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_2#10" accession="ERX2664038">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B2, constructed from sample accession ERS1888163 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_2).  This submission includes reads tagged with the sequence TTCGCCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888163">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_2#18" accession="ERX2664039">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B3, constructed from sample accession ERS1888215 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_2).  This submission includes reads tagged with the sequence CTGGCCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888215">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888215</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229197</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_2#21" accession="ERX2664040">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E3, constructed from sample accession ERS1888220 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_2).  This submission includes reads tagged with the sequence CGCTATTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888220">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888220</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229202</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:E3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="203" NOMINAL_SDEV="45"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_2#24" accession="ERX2664041">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H3, constructed from sample accession ERS1888231 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_2).  This submission includes reads tagged with the sequence TTCGAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="467" NOMINAL_SDEV="122"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_3#1" accession="ERX2664042">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A1, constructed from sample accession ERS1887968 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_3).  This submission includes reads tagged with the sequence AATCGTTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1887968">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1887968</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104228950</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:A1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="435" NOMINAL_SDEV="65"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_3#4" accession="ERX2664043">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664043</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D1, constructed from sample accession ERS1888069 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_3).  This submission includes reads tagged with the sequence AAGATACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888069">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888069</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229051</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="283" NOMINAL_SDEV="101"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_3#7" accession="ERX2664044">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G1, constructed from sample accession ERS1888132 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_3).  This submission includes reads tagged with the sequence AAGTTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888132">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_3#10" accession="ERX2664045">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B2, constructed from sample accession ERS1888163 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_3).  This submission includes reads tagged with the sequence TTCGCCGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888163">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="486"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_3#13" accession="ERX2664046">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E2, constructed from sample accession ERS1888204 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_3).  This submission includes reads tagged with the sequence TTATTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888204">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888204</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229186</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_3#16" accession="ERX2664047">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H2, constructed from sample accession ERS1888209 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_3).  This submission includes reads tagged with the sequence GGACAACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888209">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888209</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229191</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_3#24" accession="ERX2664048">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H3, constructed from sample accession ERS1888231 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_3).  This submission includes reads tagged with the sequence TTCGAACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888231">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888231</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229213</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:H3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="468" NOMINAL_SDEV="126"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#1" accession="ERX2664049">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:C4, constructed from sample accession ERS1888249 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence TGAGTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888249">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888249</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229231</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#4" accession="ERX2664050">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:F4, constructed from sample accession ERS1888278 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence CAATGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#7" accession="ERX2664051">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A5, constructed from sample accession ERS1888289 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence CGAAGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="218" NOMINAL_SDEV="110"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#10" accession="ERX2664052">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D5, constructed from sample accession ERS1888296 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170" NOMINAL_SDEV="19"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#13" accession="ERX2664053">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G5, constructed from sample accession ERS1888305 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence TGACTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#16" accession="ERX2664054">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B6, constructed from sample accession ERS1888321 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="183" NOMINAL_SDEV="16"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#19" accession="ERX2664055">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E6, constructed from sample accession ERS1888325 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence TCACCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_4#22" accession="ERX2664056">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H6, constructed from sample accession ERS1888330 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_4).  This submission includes reads tagged with the sequence CAATCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#4" accession="ERX2664057">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:F4, constructed from sample accession ERS1888278 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence CAATGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888278">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229260</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:F4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="428"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#7" accession="ERX2664058">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A5, constructed from sample accession ERS1888289 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence CGAAGGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888289">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229271</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:A5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="224" NOMINAL_SDEV="108"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#10" accession="ERX2664059">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D5, constructed from sample accession ERS1888296 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="162" NOMINAL_SDEV="13"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#13" accession="ERX2664060">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G5, constructed from sample accession ERS1888305 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence TGACTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#16" accession="ERX2664061">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B6, constructed from sample accession ERS1888321 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="184" NOMINAL_SDEV="16"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#19" accession="ERX2664062">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E6, constructed from sample accession ERS1888325 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence TCACCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#22" accession="ERX2664063">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H6, constructed from sample accession ERS1888330 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence CAATCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_5#25" accession="ERX2664064">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:C7, constructed from sample accession ERS1888341 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_5).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="166" NOMINAL_SDEV="9"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_6#2" accession="ERX2664065">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D4, constructed from sample accession ERS1888266 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_6).  This submission includes reads tagged with the sequence CGAGCCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888266">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229248</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="239" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_6#10" accession="ERX2664066">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D5, constructed from sample accession ERS1888296 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_6).  This submission includes reads tagged with the sequence CGATTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888296">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229278</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:D5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="172" NOMINAL_SDEV="11"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_6#13" accession="ERX2664067">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G5, constructed from sample accession ERS1888305 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_6).  This submission includes reads tagged with the sequence TGACTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888305">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229287</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_6#16" accession="ERX2664068">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B6, constructed from sample accession ERS1888321 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_6).  This submission includes reads tagged with the sequence GAAGCACA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888321">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="187" NOMINAL_SDEV="17"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_6#19" accession="ERX2664069">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E6, constructed from sample accession ERS1888325 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_6).  This submission includes reads tagged with the sequence TCACCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888325">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_6#22" accession="ERX2664070">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:H6, constructed from sample accession ERS1888330 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_6).  This submission includes reads tagged with the sequence CAATCGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888330">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229312</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25155_6#25" accession="ERX2664071">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25155_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25155_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:C7, constructed from sample accession ERS1888341 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25155_6).  This submission includes reads tagged with the sequence CTTATGAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888341">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229323</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:C7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="158" NOMINAL_SDEV="20"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25163_1#2" accession="ERX2664072">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25163_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25163_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:F7, constructed from sample accession ERS1888347 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25163_1).  This submission includes reads tagged with the sequence CAACCGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888347">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229329</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25163_1#5" accession="ERX2664073">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25163_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25163_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:A8, constructed from sample accession ERS1888351 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25163_1).  This submission includes reads tagged with the sequence GATGCGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888351">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229333</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25163_1#8" accession="ERX2664074">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25163_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25163_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D8, constructed from sample accession ERS1888367 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25163_1).  This submission includes reads tagged with the sequence CGCGCCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888367">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229349</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25163_1#16" accession="ERX2664075">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25163_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25163_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:D9, constructed from sample accession ERS1888445 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25163_1).  This submission includes reads tagged with the sequence CGAACGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888445">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H: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>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25163_1#19" accession="ERX2664076">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25163_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25163_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:G9, constructed from sample accession ERS1888504 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25163_1).  This submission includes reads tagged with the sequence TGAACAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888504">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888504</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:G9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="286" NOMINAL_SDEV="59"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25163_1#22" accession="ERX2664077">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25163_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25163_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:B10, constructed from sample accession ERS1888507 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25163_1).  This submission includes reads tagged with the sequence CGGATAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888507">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888507</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229489</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:B10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="214"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_25163_1#25" accession="ERX2664078">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX2664078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_25163_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_25163_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP000195">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000195</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB2141</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library DN504550H:E10, constructed from sample accession ERS1888512 for study accession ERP000195.  This is part of an Illumina multiplexed sequencing run (25163_1).  This submission includes reads tagged with the sequence TCAACGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS1888512">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS1888512</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA104229494</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>DN504550H:E10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320" NOMINAL_SDEV="203"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>HiSeqX PCR free</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
